Canonical Allele Identifier: CA490946353

Gene: ITGA11

Linked Data

• MyVariant Identifiers: chr15:g.68628167C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335829C>G , CM000677.2:g.68335829C>G	GRCh38
NC_000015.9:g.68628167C>G , CM000677.1:g.68628167C>G	GRCh37
NC_000015.8:g.66415221C>G	NCBI36
NG_046911.1:g.101332G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000315757.9:c.1293G>C MANE Select	ENSP00000327290.7:p.Ser431=
ENST00000315757.8:c.1293G>C	ENSP00000327290.7:p.Ser431=
ENST00000423218.6:c.1293G>C	ENSP00000403392.2:p.Ser431=
ENST00000566429.1:n.197-15G>C
ENST00000569346.5:n.272G>C
NM_001004439.1:c.1293G>C	NP_001004439.1:p.Ser431=
XM_005254228.2:c.987G>C	XP_005254285.1:p.Ser329=
XM_011521363.1:c.1086G>C	XP_011519665.1:p.Ser362=
XM_005254228.3:c.987G>C	XP_005254285.1:p.Ser329=
XM_011521363.2:c.1086G>C	XP_011519665.1:p.Ser362=
NM_001004439.2:c.1293G>C MANE Select	NP_001004439.1:p.Ser431=