Canonical Allele Identifier: CA385181809

Gene: ITGA7

Linked Data

• MyVariant Identifiers: chr12:g.56087086G>A (hg19) ; chr12:g.55693302G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55693302G>A , CM000674.2:g.55693302G>A	GRCh38
NC_000012.11:g.56087086G>A , CM000674.1:g.56087086G>A	GRCh37
NC_000012.10:g.54373353G>A	NCBI36
NG_012343.1:g.24004C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553893.6:c.*2175C>T	ENSP00000452467.1:n.*2175C>T
ENST00000554327.6:c.1222C>T
ENST00000557058.2:n.1966C>T
ENST00000557257.2:c.2077C>T	ENSP00000450578.2:p.Gln693Ter
ENST00000557555.3:c.2563C>T	ENSP00000451039.3:p.Gln855Ter
ENST00000686981.1:c.*2262C>T	ENSP00000510795.1:n.*2262C>T
ENST00000687390.1:n.657C>T
ENST00000691052.1:c.*1035C>T	ENSP00000508886.1:n.*1035C>T
ENST00000691846.1:c.1364C>T
ENST00000691973.1:c.2563C>T	ENSP00000509141.1:p.Gln855Ter
ENST00000257879.11:c.2551C>T MANE Select	ENSP00000257879.7:p.Gln851Ter
ENST00000553804.6:c.2563C>T	ENSP00000452120.1:p.Gln855Ter
ENST00000257879.10:c.2551C>T	ENSP00000257879.6:p.Gln851Ter
ENST00000347027.10:c.2533C>T	ENSP00000343009.6:p.Gln845Ter
ENST00000452168.6:c.2272C>T	ENSP00000393844.2:p.Gln758Ter
ENST00000553804.5:c.2563C>T	ENSP00000452120.1:p.Gln855Ter
ENST00000554327.5:c.616C>T
ENST00000555728.5:c.2683C>T	ENSP00000452387.1:p.Gln895Ter
NM_001144996.1:c.2563C>T	NP_001138468.1:p.Gln855Ter
NM_001144997.1:c.2272C>T	NP_001138469.1:p.Gln758Ter
NM_002206.2:c.2551C>T	NP_002197.2:p.Gln851Ter
XM_005268839.1:c.2683C>T	XP_005268896.1:p.Gln895Ter
XM_005268840.1:c.2665C>T	XP_005268897.1:p.Gln889Ter
XM_005268841.1:c.2683C>T	XP_005268898.1:p.Gln895Ter
XM_005268842.1:c.2533C>T	XP_005268899.1:p.Gln845Ter
XM_005268844.1:c.2344C>T	XP_005268901.1:p.Gln782Ter
XM_005268845.1:c.2212C>T	XP_005268902.1:p.Gln738Ter
XM_005268846.1:c.2212C>T	XP_005268903.1:p.Gln738Ter
XM_005268847.1:c.2209C>T	XP_005268904.1:p.Gln737Ter
XM_005268848.1:c.2209C>T	XP_005268905.1:p.Gln737Ter
XM_005268849.1:c.2209C>T	XP_005268906.1:p.Gln737Ter
XM_005268850.1:c.2077C>T	XP_005268907.1:p.Gln693Ter
XM_011538286.1:c.2344C>T	XP_011536588.1:p.Gln782Ter
XM_005268839.2:c.2683C>T	XP_005268896.1:p.Gln895Ter
XM_005268840.2:c.2665C>T	XP_005268897.1:p.Gln889Ter
XM_005268841.2:c.2683C>T	XP_005268898.1:p.Gln895Ter
XM_005268842.2:c.2533C>T	XP_005268899.1:p.Gln845Ter
XM_017019265.1:c.2293C>T	XP_016874754.1:p.Gln765Ter
NM_001144996.2:c.2563C>T	NP_001138468.1:p.Gln855Ter
NM_001367993.1:c.2224C>T	NP_001354922.1:p.Gln742Ter
NM_001367994.1:c.1207C>T	NP_001354923.1:p.Gln403Ter
NM_001374465.1:c.2533C>T	NP_001361394.1:p.Gln845Ter
NM_002206.3:c.2551C>T MANE Select	NP_002197.2:p.Gln851Ter