Canonical Allele Identifier: CA385181754

Gene: ITGA7

Linked Data

• MyVariant Identifiers: chr12:g.56087058A>G (hg19) ; chr12:g.55693274A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55693274A>G , CM000674.2:g.55693274A>G	GRCh38
NC_000012.11:g.56087058A>G , CM000674.1:g.56087058A>G	GRCh37
NC_000012.10:g.54373325A>G	NCBI36
NG_012343.1:g.24032T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553893.6:c.*2203T>C	ENSP00000452467.1:n.*2203T>C
ENST00000554327.6:c.1250T>C
ENST00000557058.2:n.1994T>C
ENST00000557257.2:c.2105T>C	ENSP00000450578.2:p.Phe702Ser
ENST00000557555.3:c.2591T>C	ENSP00000451039.3:p.Phe864Ser
ENST00000686981.1:c.*2290T>C	ENSP00000510795.1:n.*2290T>C
ENST00000687390.1:n.685T>C
ENST00000691052.1:c.*1063T>C	ENSP00000508886.1:n.*1063T>C
ENST00000691846.1:c.1392T>C
ENST00000691973.1:c.2591T>C	ENSP00000509141.1:p.Phe864Ser
ENST00000257879.11:c.2579T>C MANE Select	ENSP00000257879.7:p.Phe860Ser
ENST00000553804.6:c.2591T>C	ENSP00000452120.1:p.Phe864Ser
ENST00000257879.10:c.2579T>C	ENSP00000257879.6:p.Phe860Ser
ENST00000347027.10:c.2561T>C	ENSP00000343009.6:p.Phe854Ser
ENST00000452168.6:c.2300T>C	ENSP00000393844.2:p.Phe767Ser
ENST00000553804.5:c.2591T>C	ENSP00000452120.1:p.Phe864Ser
ENST00000554327.5:c.644T>C
ENST00000555728.5:c.2711T>C	ENSP00000452387.1:p.Phe904Ser
NM_001144996.1:c.2591T>C	NP_001138468.1:p.Phe864Ser
NM_001144997.1:c.2300T>C	NP_001138469.1:p.Phe767Ser
NM_002206.2:c.2579T>C	NP_002197.2:p.Phe860Ser
XM_005268839.1:c.2711T>C	XP_005268896.1:p.Phe904Ser
XM_005268840.1:c.2693T>C	XP_005268897.1:p.Phe898Ser
XM_005268841.1:c.2711T>C	XP_005268898.1:p.Phe904Ser
XM_005268842.1:c.2561T>C	XP_005268899.1:p.Phe854Ser
XM_005268844.1:c.2372T>C	XP_005268901.1:p.Phe791Ser
XM_005268845.1:c.2240T>C	XP_005268902.1:p.Phe747Ser
XM_005268846.1:c.2240T>C	XP_005268903.1:p.Phe747Ser
XM_005268847.1:c.2237T>C	XP_005268904.1:p.Phe746Ser
XM_005268848.1:c.2237T>C	XP_005268905.1:p.Phe746Ser
XM_005268849.1:c.2237T>C	XP_005268906.1:p.Phe746Ser
XM_005268850.1:c.2105T>C	XP_005268907.1:p.Phe702Ser
XM_011538286.1:c.2372T>C	XP_011536588.1:p.Phe791Ser
XM_005268839.2:c.2711T>C	XP_005268896.1:p.Phe904Ser
XM_005268840.2:c.2693T>C	XP_005268897.1:p.Phe898Ser
XM_005268841.2:c.2711T>C	XP_005268898.1:p.Phe904Ser
XM_005268842.2:c.2561T>C	XP_005268899.1:p.Phe854Ser
XM_017019265.1:c.2321T>C	XP_016874754.1:p.Phe774Ser
NM_001144996.2:c.2591T>C	NP_001138468.1:p.Phe864Ser
NM_001367993.1:c.2252T>C	NP_001354922.1:p.Phe751Ser
NM_001367994.1:c.1235T>C	NP_001354923.1:p.Phe412Ser
NM_001374465.1:c.2561T>C	NP_001361394.1:p.Phe854Ser
NM_002206.3:c.2579T>C MANE Select	NP_002197.2:p.Phe860Ser