Canonical Allele Identifier: CA6782106

Gene: GIT2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109988999C>T , CM000674.2:g.109988999C>T	GRCh38
NC_000012.11:g.110426804C>T , CM000674.1:g.110426804C>T	GRCh37
NC_000012.10:g.108911187C>T	NCBI36
NG_029885.1:g.12391G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355312.8:c.369G>A MANE Select	ENSP00000347464.3:p.Arg123=
ENST00000320063.10:c.369G>A	ENSP00000323833.9:p.Arg123=
ENST00000354574.8:c.369G>A	ENSP00000346585.4:p.Arg123=
ENST00000355312.7:c.369G>A	ENSP00000347464.3:p.Arg123=
ENST00000361006.9:c.369G>A	ENSP00000354282.5:p.Arg123=
ENST00000457474.6:c.369G>A	ENSP00000391813.2:p.Arg123=
ENST00000547267.2:n.645G>A
ENST00000547815.5:c.369G>A	ENSP00000450348.1:p.Arg123=
ENST00000548643.5:n.587G>A
ENST00000550186.5:c.183G>A	ENSP00000473637.1:p.Arg61=
ENST00000551209.5:c.369G>A	ENSP00000448832.1:p.Arg123=
ENST00000551455.5:n.518G>A
ENST00000553118.5:c.369G>A	ENSP00000447465.1:p.Arg123=
NM_001135213.1:c.369G>A	NP_001128685.1:p.Arg123=
NM_001135214.1:c.369G>A	NP_001128686.1:p.Arg123=
NM_014776.3:c.369G>A	NP_055591.2:p.Arg123=
NM_057169.3:c.369G>A	NP_476510.1:p.Arg123=
NM_057170.3:c.369G>A	NP_476511.1:p.Arg123=
NM_139201.2:c.369G>A	NP_631940.2:p.Arg123=
XM_005253997.2:c.369G>A	XP_005254054.1:p.Arg123=
XM_005254000.2:c.369G>A	XP_005254057.1:p.Arg123=
XM_006719707.2:c.369G>A	XP_006719770.1:p.Arg123=
XM_006719708.2:c.369G>A	XP_006719771.1:p.Arg123=
XM_006719709.2:c.369G>A	XP_006719772.1:p.Arg123=
XM_006719712.2:c.369G>A	XP_006719775.1:p.Arg123=
XM_006719713.2:c.369G>A	XP_006719776.1:p.Arg123=
XM_006719714.2:c.369G>A	XP_006719777.1:p.Arg123=
NM_001135213.2:c.369G>A	NP_001128685.1:p.Arg123=
NM_001135214.2:c.369G>A	NP_001128686.1:p.Arg123=
NM_001330153.1:c.369G>A	NP_001317082.1:p.Arg123=
NM_001330154.1:c.369G>A	NP_001317083.1:p.Arg123=
NM_014776.4:c.369G>A	NP_055591.2:p.Arg123=
NM_057169.4:c.369G>A	NP_476510.1:p.Arg123=
NM_057170.4:c.369G>A	NP_476511.1:p.Arg123=
XM_005253997.4:c.369G>A	XP_005254054.1:p.Arg123=
XM_006719707.4:c.369G>A	XP_006719770.1:p.Arg123=
XM_006719708.4:c.369G>A	XP_006719771.1:p.Arg123=
XM_006719709.4:c.369G>A	XP_006719772.1:p.Arg123=
XM_006719712.4:c.369G>A	XP_006719775.1:p.Arg123=
XM_006719713.4:c.369G>A	XP_006719776.1:p.Arg123=
XM_017020258.2:c.369G>A	XP_016875747.1:p.Arg123=
XM_017020259.2:c.369G>A	XP_016875748.1:p.Arg123=
XM_017020260.2:c.369G>A	XP_016875749.1:p.Arg123=
XM_017020261.2:c.369G>A	XP_016875750.1:p.Arg123=
NM_057169.5:c.369G>A MANE Select	NP_476510.1:p.Arg123=
NM_001135213.3:c.369G>A	NP_001128685.1:p.Arg123=
NM_001135214.3:c.369G>A	NP_001128686.1:p.Arg123=
NM_001330153.2:c.369G>A	NP_001317082.1:p.Arg123=
NM_001330154.2:c.369G>A	NP_001317083.1:p.Arg123=
NM_014776.5:c.369G>A	NP_055591.2:p.Arg123=
NM_057170.5:c.369G>A	NP_476511.1:p.Arg123=
NM_139201.3:c.369G>A	NP_631940.2:p.Arg123=