Canonical Allele Identifier: CA480145569

Gene: ITGA7

Linked Data

• MyVariant Identifiers: chr12:g.56087063A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55693279A>T , CM000674.2:g.55693279A>T	GRCh38
NC_000012.11:g.56087063A>T , CM000674.1:g.56087063A>T	GRCh37
NC_000012.10:g.54373330A>T	NCBI36
NG_012343.1:g.24027T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553893.6:c.*2198T>A	ENSP00000452467.1:n.*2198T>A
ENST00000554327.6:c.1245T>A
ENST00000557058.2:n.1989T>A
ENST00000557257.2:c.2100T>A	ENSP00000450578.2:p.Ser700=
ENST00000557555.3:c.2586T>A	ENSP00000451039.3:p.Ser862=
ENST00000686981.1:c.*2285T>A	ENSP00000510795.1:n.*2285T>A
ENST00000687390.1:n.680T>A
ENST00000691052.1:c.*1058T>A	ENSP00000508886.1:n.*1058T>A
ENST00000691846.1:c.1387T>A
ENST00000691973.1:c.2586T>A	ENSP00000509141.1:p.Ser862=
ENST00000257879.11:c.2574T>A MANE Select	ENSP00000257879.7:p.Ser858=
ENST00000553804.6:c.2586T>A	ENSP00000452120.1:p.Ser862=
ENST00000257879.10:c.2574T>A	ENSP00000257879.6:p.Ser858=
ENST00000347027.10:c.2556T>A	ENSP00000343009.6:p.Ser852=
ENST00000452168.6:c.2295T>A	ENSP00000393844.2:p.Ser765=
ENST00000553804.5:c.2586T>A	ENSP00000452120.1:p.Ser862=
ENST00000554327.5:c.639T>A
ENST00000555728.5:c.2706T>A	ENSP00000452387.1:p.Ser902=
NM_001144996.1:c.2586T>A	NP_001138468.1:p.Ser862=
NM_001144997.1:c.2295T>A	NP_001138469.1:p.Ser765=
NM_002206.2:c.2574T>A	NP_002197.2:p.Ser858=
XM_005268839.1:c.2706T>A	XP_005268896.1:p.Ser902=
XM_005268840.1:c.2688T>A	XP_005268897.1:p.Ser896=
XM_005268841.1:c.2706T>A	XP_005268898.1:p.Ser902=
XM_005268842.1:c.2556T>A	XP_005268899.1:p.Ser852=
XM_005268844.1:c.2367T>A	XP_005268901.1:p.Ser789=
XM_005268845.1:c.2235T>A	XP_005268902.1:p.Ser745=
XM_005268846.1:c.2235T>A	XP_005268903.1:p.Ser745=
XM_005268847.1:c.2232T>A	XP_005268904.1:p.Ser744=
XM_005268848.1:c.2232T>A	XP_005268905.1:p.Ser744=
XM_005268849.1:c.2232T>A	XP_005268906.1:p.Ser744=
XM_005268850.1:c.2100T>A	XP_005268907.1:p.Ser700=
XM_011538286.1:c.2367T>A	XP_011536588.1:p.Ser789=
XM_005268839.2:c.2706T>A	XP_005268896.1:p.Ser902=
XM_005268840.2:c.2688T>A	XP_005268897.1:p.Ser896=
XM_005268841.2:c.2706T>A	XP_005268898.1:p.Ser902=
XM_005268842.2:c.2556T>A	XP_005268899.1:p.Ser852=
XM_017019265.1:c.2316T>A	XP_016874754.1:p.Ser772=
NM_001144996.2:c.2586T>A	NP_001138468.1:p.Ser862=
NM_001367993.1:c.2247T>A	NP_001354922.1:p.Ser749=
NM_001367994.1:c.1230T>A	NP_001354923.1:p.Ser410=
NM_001374465.1:c.2556T>A	NP_001361394.1:p.Ser852=
NM_002206.3:c.2574T>A MANE Select	NP_002197.2:p.Ser858=