Canonical Allele Identifier: CA392977878

Gene: ITGA11

Linked Data

• MyVariant Identifiers: chr15:g.68628142C>T (hg19) ; chr15:g.68335804C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335804C>T , CM000677.2:g.68335804C>T	GRCh38
NC_000015.9:g.68628142C>T , CM000677.1:g.68628142C>T	GRCh37
NC_000015.8:g.66415196C>T	NCBI36
NG_046911.1:g.101357G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1318G>A MANE Select	ENSP00000327290.7:p.Val440Met
ENST00000315757.8:c.1318G>A	ENSP00000327290.7:p.Val440Met
ENST00000423218.6:c.1318G>A	ENSP00000403392.2:p.Val440Met
ENST00000566429.1:n.207G>A
ENST00000569346.5:n.297G>A
NM_001004439.1:c.1318G>A	NP_001004439.1:p.Val440Met
XM_005254228.2:c.1012G>A	XP_005254285.1:p.Val338Met
XM_011521363.1:c.1111G>A	XP_011519665.1:p.Val371Met
XM_005254228.3:c.1012G>A	XP_005254285.1:p.Val338Met
XM_011521363.2:c.1111G>A	XP_011519665.1:p.Val371Met
NM_001004439.2:c.1318G>A MANE Select	NP_001004439.1:p.Val440Met