Canonical Allele Identifier: CA480145663

Gene: ITGA7

Linked Data

• MyVariant Identifiers: chr12:g.56087093G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55693309G>A , CM000674.2:g.55693309G>A	GRCh38
NC_000012.11:g.56087093G>A , CM000674.1:g.56087093G>A	GRCh37
NC_000012.10:g.54373360G>A	NCBI36
NG_012343.1:g.23997C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553893.6:c.*2168C>T	ENSP00000452467.1:n.*2168C>T
ENST00000554327.6:c.1215C>T
ENST00000557058.2:n.1959C>T
ENST00000557257.2:c.2070C>T	ENSP00000450578.2:p.Asn690=
ENST00000557555.3:c.2556C>T	ENSP00000451039.3:p.Asn852=
ENST00000686981.1:c.*2255C>T	ENSP00000510795.1:n.*2255C>T
ENST00000687390.1:n.650C>T
ENST00000691052.1:c.*1028C>T	ENSP00000508886.1:n.*1028C>T
ENST00000691846.1:c.1357C>T
ENST00000691973.1:c.2556C>T	ENSP00000509141.1:p.Asn852=
ENST00000257879.11:c.2544C>T MANE Select	ENSP00000257879.7:p.Asn848=
ENST00000553804.6:c.2556C>T	ENSP00000452120.1:p.Asn852=
ENST00000257879.10:c.2544C>T	ENSP00000257879.6:p.Asn848=
ENST00000347027.10:c.2526C>T	ENSP00000343009.6:p.Asn842=
ENST00000452168.6:c.2265C>T	ENSP00000393844.2:p.Asn755=
ENST00000553804.5:c.2556C>T	ENSP00000452120.1:p.Asn852=
ENST00000554327.5:c.609C>T
ENST00000555728.5:c.2676C>T	ENSP00000452387.1:p.Asn892=
NM_001144996.1:c.2556C>T	NP_001138468.1:p.Asn852=
NM_001144997.1:c.2265C>T	NP_001138469.1:p.Asn755=
NM_002206.2:c.2544C>T	NP_002197.2:p.Asn848=
XM_005268839.1:c.2676C>T	XP_005268896.1:p.Asn892=
XM_005268840.1:c.2658C>T	XP_005268897.1:p.Asn886=
XM_005268841.1:c.2676C>T	XP_005268898.1:p.Asn892=
XM_005268842.1:c.2526C>T	XP_005268899.1:p.Asn842=
XM_005268844.1:c.2337C>T	XP_005268901.1:p.Asn779=
XM_005268845.1:c.2205C>T	XP_005268902.1:p.Asn735=
XM_005268846.1:c.2205C>T	XP_005268903.1:p.Asn735=
XM_005268847.1:c.2202C>T	XP_005268904.1:p.Asn734=
XM_005268848.1:c.2202C>T	XP_005268905.1:p.Asn734=
XM_005268849.1:c.2202C>T	XP_005268906.1:p.Asn734=
XM_005268850.1:c.2070C>T	XP_005268907.1:p.Asn690=
XM_011538286.1:c.2337C>T	XP_011536588.1:p.Asn779=
XM_005268839.2:c.2676C>T	XP_005268896.1:p.Asn892=
XM_005268840.2:c.2658C>T	XP_005268897.1:p.Asn886=
XM_005268841.2:c.2676C>T	XP_005268898.1:p.Asn892=
XM_005268842.2:c.2526C>T	XP_005268899.1:p.Asn842=
XM_017019265.1:c.2286C>T	XP_016874754.1:p.Asn762=
NM_001144996.2:c.2556C>T	NP_001138468.1:p.Asn852=
NM_001367993.1:c.2217C>T	NP_001354922.1:p.Asn739=
NM_001367994.1:c.1200C>T	NP_001354923.1:p.Asn400=
NM_001374465.1:c.2526C>T	NP_001361394.1:p.Asn842=
NM_002206.3:c.2544C>T MANE Select	NP_002197.2:p.Asn848=