Canonical Allele Identifier: CA480145203

Gene: ITGA7

Linked Data

• MyVariant Identifiers: chr12:g.56086946G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55693162G>A , CM000674.2:g.55693162G>A	GRCh38
NC_000012.11:g.56086946G>A , CM000674.1:g.56086946G>A	GRCh37
NC_000012.10:g.54373213G>A	NCBI36
NG_012343.1:g.24144C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553893.6:c.*2315C>T	ENSP00000452467.1:n.*2315C>T
ENST00000554327.6:c.1362C>T
ENST00000557058.2:n.2106C>T
ENST00000557257.2:c.2217C>T	ENSP00000450578.2:p.Pro739=
ENST00000557555.3:c.2703C>T	ENSP00000451039.3:p.Pro901=
ENST00000686981.1:c.*2402C>T	ENSP00000510795.1:n.*2402C>T
ENST00000687390.1:n.797C>T
ENST00000691052.1:c.*1175C>T	ENSP00000508886.1:n.*1175C>T
ENST00000691846.1:c.1504C>T
ENST00000691973.1:c.2652+51C>T	ENSP00000509141.1:n.2652+51C>T
ENST00000257879.11:c.2691C>T MANE Select	ENSP00000257879.7:p.Pro897=
ENST00000553804.6:c.2703C>T	ENSP00000452120.1:p.Pro901=
ENST00000257879.10:c.2691C>T	ENSP00000257879.6:p.Pro897=
ENST00000347027.10:c.2673C>T	ENSP00000343009.6:p.Pro891=
ENST00000452168.6:c.2412C>T	ENSP00000393844.2:p.Pro804=
ENST00000553804.5:c.2703C>T	ENSP00000452120.1:p.Pro901=
ENST00000554327.5:c.756C>T
ENST00000555728.5:c.2823C>T	ENSP00000452387.1:p.Pro941=
NM_001144996.1:c.2703C>T	NP_001138468.1:p.Pro901=
NM_001144997.1:c.2412C>T	NP_001138469.1:p.Pro804=
NM_002206.2:c.2691C>T	NP_002197.2:p.Pro897=
XM_005268839.1:c.2823C>T	XP_005268896.1:p.Pro941=
XM_005268840.1:c.2805C>T	XP_005268897.1:p.Pro935=
XM_005268841.1:c.2823C>T	XP_005268898.1:p.Pro941=
XM_005268842.1:c.2673C>T	XP_005268899.1:p.Pro891=
XM_005268844.1:c.2484C>T	XP_005268901.1:p.Pro828=
XM_005268845.1:c.2352C>T	XP_005268902.1:p.Pro784=
XM_005268846.1:c.2352C>T	XP_005268903.1:p.Pro784=
XM_005268847.1:c.2349C>T	XP_005268904.1:p.Pro783=
XM_005268848.1:c.2349C>T	XP_005268905.1:p.Pro783=
XM_005268849.1:c.2349C>T	XP_005268906.1:p.Pro783=
XM_005268850.1:c.2217C>T	XP_005268907.1:p.Pro739=
XM_011538286.1:c.2484C>T	XP_011536588.1:p.Pro828=
XM_005268839.2:c.2823C>T	XP_005268896.1:p.Pro941=
XM_005268840.2:c.2805C>T	XP_005268897.1:p.Pro935=
XM_005268841.2:c.2823C>T	XP_005268898.1:p.Pro941=
XM_005268842.2:c.2673C>T	XP_005268899.1:p.Pro891=
XM_017019265.1:c.2433C>T	XP_016874754.1:p.Pro811=
NM_001144996.2:c.2703C>T	NP_001138468.1:p.Pro901=
NM_001367993.1:c.2364C>T	NP_001354922.1:p.Pro788=
NM_001367994.1:c.1347C>T	NP_001354923.1:p.Pro449=
NM_001374465.1:c.2673C>T	NP_001361394.1:p.Pro891=
NM_002206.3:c.2691C>T MANE Select	NP_002197.2:p.Pro897=