Canonical Allele Identifier: CA2119208536

Gene: ARHGEF7

Linked Data

• dbSNP Id: rs4773330

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.111166485A>T , CM000675.2:g.111166485A>T	GRCh38
NC_000013.10:g.111818832A>T , CM000675.1:g.111818832A>T	GRCh37
NC_000013.9:g.110616833A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000700426.1:c.252+12494A>T	ENSP00000514984.1:n.252+12494A>T
ENST00000646102.2:c.252+12494A>T MANE Select	ENSP00000495631.1:n.252+12494A>T
ENST00000646102.1:c.252+12494A>T	ENSP00000495631.1:n.252+12494A>T
ENST00000218789.9:c.-220+12494A>T	ENSP00000218789.5:n.-220+12494A>T
ENST00000317133.9:c.252+12494A>T	ENSP00000325994.5:n.252+12494A>T
ENST00000375736.8:c.-220+12494A>T	ENSP00000364888.4:n.-220+12494A>T
ENST00000375739.6:c.166-38804A>T	ENSP00000364891.2:n.166-38804A>T
ENST00000375741.6:c.315+7396A>T	ENSP00000364893.2:n.315+7396A>T
ENST00000449979.5:c.-219-38804A>T	ENSP00000406732.1:n.-219-38804A>T
ENST00000466143.5:c.-220+12494A>T	ENSP00000418067.1:n.-220+12494A>T
ENST00000469877.5:c.-89+12494A>T	ENSP00000418235.1:n.-89+12494A>T
ENST00000491775.5:c.-301+12494A>T	ENSP00000418043.1:n.-301+12494A>T
NM_001113511.1:c.315+7396A>T	NP_001106983.1:n.315+7396A>T
NM_001113512.1:c.166-38804A>T	NP_001106984.1:n.166-38804A>T
NM_003899.3:c.-220+12494A>T	NP_003890.1:n.-220+12494A>T
NM_145735.2:c.252+12494A>T	NP_663788.1:n.252+12494A>T
XM_005254085.2:c.252+12494A>T	XP_005254142.1:n.252+12494A>T
XM_005254086.2:c.252+12494A>T	XP_005254143.1:n.252+12494A>T
XM_005254087.2:c.252+12494A>T	XP_005254144.1:n.252+12494A>T
XM_005254088.2:c.252+12494A>T	XP_005254145.1:n.252+12494A>T
XM_005254090.2:c.252+12494A>T	XP_005254147.1:n.252+12494A>T
XM_005254092.2:c.-220+12494A>T	XP_005254149.1:n.-220+12494A>T
XM_005254094.2:c.-89+12494A>T	XP_005254151.1:n.-89+12494A>T
XM_005254095.2:c.-4+12494A>T	XP_005254152.1:n.-4+12494A>T
XM_006719956.2:c.252+12494A>T	XP_006720019.1:n.252+12494A>T
XM_006719960.2:c.252+12494A>T	XP_006720023.1:n.252+12494A>T
XM_011521130.1:c.166-38804A>T	XP_011519432.1:n.166-38804A>T
XM_011521131.1:c.166-38804A>T	XP_011519433.1:n.166-38804A>T
XM_011521132.1:c.-232+12494A>T	XP_011519434.1:n.-232+12494A>T
XM_011521133.1:c.252+12494A>T	XP_011519435.1:n.252+12494A>T
NM_001113511.2:c.315+7396A>T	NP_001106983.1:n.315+7396A>T
NM_001113512.2:c.166-38804A>T	NP_001106984.1:n.166-38804A>T
NM_001320851.1:c.-4+12494A>T	NP_001307780.1:n.-4+12494A>T
NM_001320852.1:c.252+12494A>T	NP_001307781.1:n.252+12494A>T
NM_001330597.1:c.-220+12494A>T	NP_001317526.1:n.-220+12494A>T
NM_001330598.1:c.-4+12494A>T	NP_001317527.1:n.-4+12494A>T
NM_001354046.1:c.252+12494A>T	NP_001340975.1:n.252+12494A>T
NM_001354047.1:c.252+12494A>T	NP_001340976.1:n.252+12494A>T
NM_001354048.1:c.-220+12494A>T	NP_001340977.1:n.-220+12494A>T
NM_001354049.1:c.-220+12494A>T	NP_001340978.1:n.-220+12494A>T
NM_001354050.1:c.-135+12494A>T	NP_001340979.1:n.-135+12494A>T
NM_001354051.1:c.-220+12494A>T	NP_001340980.1:n.-220+12494A>T
NM_001354052.1:c.-220+12494A>T	NP_001340981.1:n.-220+12494A>T
NM_001354053.1:c.-4+12494A>T	NP_001340982.1:n.-4+12494A>T
NM_001354054.1:c.-220+12494A>T	NP_001340983.1:n.-220+12494A>T
NM_001354056.1:c.-4+12494A>T	NP_001340985.1:n.-4+12494A>T
NM_001354057.1:c.-135+7396A>T	NP_001340986.1:n.-135+7396A>T
NM_001354058.1:c.-232+12494A>T	NP_001340987.1:n.-232+12494A>T
NM_001354059.1:c.-220+7396A>T	NP_001340988.1:n.-220+7396A>T
NM_001354060.1:c.-220+12494A>T	NP_001340989.1:n.-220+12494A>T
NM_003899.4:c.-220+12494A>T	NP_003890.1:n.-220+12494A>T
NM_145735.3:c.252+12494A>T	NP_663788.1:n.252+12494A>T
XM_006719956.3:c.252+12494A>T	XP_006720019.1:n.252+12494A>T
XM_011521133.2:c.252+12494A>T	XP_011519435.1:n.252+12494A>T
XM_017020814.1:c.252+12494A>T	XP_016876303.1:n.252+12494A>T
XM_017020815.1:c.252+12494A>T	XP_016876304.1:n.252+12494A>T
XM_017020821.2:c.-89+12494A>T	XP_016876310.1:n.-89+12494A>T
XM_017020822.1:c.-4+12494A>T	XP_016876311.1:n.-4+12494A>T
XM_024449428.1:c.-232+12494A>T	XP_024305196.1:n.-232+12494A>T
XR_001749712.1:n.288+12494A>T
XR_002957481.1:n.497+12494A>T
NM_001320851.2:c.-4+12494A>T	NP_001307780.1:n.-4+12494A>T
NM_001330597.2:c.-220+12494A>T	NP_001317526.1:n.-220+12494A>T
NM_001330598.2:c.-4+12494A>T	NP_001317527.1:n.-4+12494A>T
NM_001354049.2:c.-220+12494A>T	NP_001340978.1:n.-220+12494A>T
NM_001354050.2:c.-135+12494A>T	NP_001340979.1:n.-135+12494A>T
NM_001354051.2:c.-220+12494A>T	NP_001340980.1:n.-220+12494A>T
NM_001354052.2:c.-220+12494A>T	NP_001340981.1:n.-220+12494A>T
NM_001354053.2:c.-4+12494A>T	NP_001340982.1:n.-4+12494A>T
NM_001354054.2:c.-220+12494A>T	NP_001340983.1:n.-220+12494A>T
NM_001354057.2:c.-135+7396A>T	NP_001340986.1:n.-135+7396A>T
NM_001354058.2:c.-232+12494A>T	NP_001340987.1:n.-232+12494A>T
NM_001354059.2:c.-220+7396A>T	NP_001340988.1:n.-220+7396A>T
NM_001354060.2:c.-220+12494A>T	NP_001340989.1:n.-220+12494A>T
NM_003899.5:c.-220+12494A>T	NP_003890.1:n.-220+12494A>T
NM_001354046.2:c.252+12494A>T MANE Select	NP_001340975.1:n.252+12494A>T