Canonical Allele Identifier: CA392977806

Gene: ITGA11

Linked Data

• MyVariant Identifiers: chr15:g.68628105C>G (hg19) ; chr15:g.68335767C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335767C>G , CM000677.2:g.68335767C>G	GRCh38
NC_000015.9:g.68628105C>G , CM000677.1:g.68628105C>G	GRCh37
NC_000015.8:g.66415159C>G	NCBI36
NG_046911.1:g.101394G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1355G>C MANE Select	ENSP00000327290.7:p.Gly452Ala
ENST00000315757.8:c.1355G>C	ENSP00000327290.7:p.Gly452Ala
ENST00000423218.6:c.1355G>C	ENSP00000403392.2:p.Gly452Ala
ENST00000566429.1:n.244G>C
ENST00000569346.5:n.334G>C
NM_001004439.1:c.1355G>C	NP_001004439.1:p.Gly452Ala
XM_005254228.2:c.1049G>C	XP_005254285.1:p.Gly350Ala
XM_011521363.1:c.1148G>C	XP_011519665.1:p.Gly383Ala
XM_005254228.3:c.1049G>C	XP_005254285.1:p.Gly350Ala
XM_011521363.2:c.1148G>C	XP_011519665.1:p.Gly383Ala
NM_001004439.2:c.1355G>C MANE Select	NP_001004439.1:p.Gly452Ala