Canonical Allele Identifier: CA7631863

Gene: ITGA11

Linked Data

• dbSNP Id: rs770522528
• ExAC: 15:68628141 A / C
• gnomAD v2: 15-68628141-A-C
• gnomAD v4: 15-68335803-A-C
• MyVariant Identifiers: chr15:g.68628141A>C (hg19) ; chr15:g.68335803A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335803A>C , CM000677.2:g.68335803A>C	GRCh38
NC_000015.9:g.68628141A>C , CM000677.1:g.68628141A>C	GRCh37
NC_000015.8:g.66415195A>C	NCBI36
NG_046911.1:g.101358T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1319T>G MANE Select	ENSP00000327290.7:p.Val440Gly
ENST00000315757.8:c.1319T>G	ENSP00000327290.7:p.Val440Gly
ENST00000423218.6:c.1319T>G	ENSP00000403392.2:p.Val440Gly
ENST00000566429.1:n.208T>G
ENST00000569346.5:n.298T>G
NM_001004439.1:c.1319T>G	NP_001004439.1:p.Val440Gly
XM_005254228.2:c.1013T>G	XP_005254285.1:p.Val338Gly
XM_011521363.1:c.1112T>G	XP_011519665.1:p.Val371Gly
XM_005254228.3:c.1013T>G	XP_005254285.1:p.Val338Gly
XM_011521363.2:c.1112T>G	XP_011519665.1:p.Val371Gly
NM_001004439.2:c.1319T>G MANE Select	NP_001004439.1:p.Val440Gly