Canonical Allele Identifier: CA392977852

Gene: ITGA11

Linked Data

• dbSNP Id: rs1485925620
• gnomAD v2: 15-68628127-C-T
• gnomAD v4: 15-68335789-C-T
• MyVariant Identifiers: chr15:g.68628127C>T (hg19) ; chr15:g.68335789C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335789C>T , CM000677.2:g.68335789C>T	GRCh38
NC_000015.9:g.68628127C>T , CM000677.1:g.68628127C>T	GRCh37
NC_000015.8:g.66415181C>T	NCBI36
NG_046911.1:g.101372G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1333G>A MANE Select	ENSP00000327290.7:p.Ala445Thr
ENST00000315757.8:c.1333G>A	ENSP00000327290.7:p.Ala445Thr
ENST00000423218.6:c.1333G>A	ENSP00000403392.2:p.Ala445Thr
ENST00000566429.1:n.222G>A
ENST00000569346.5:n.312G>A
NM_001004439.1:c.1333G>A	NP_001004439.1:p.Ala445Thr
XM_005254228.2:c.1027G>A	XP_005254285.1:p.Ala343Thr
XM_011521363.1:c.1126G>A	XP_011519665.1:p.Ala376Thr
XM_005254228.3:c.1027G>A	XP_005254285.1:p.Ala343Thr
XM_011521363.2:c.1126G>A	XP_011519665.1:p.Ala376Thr
NM_001004439.2:c.1333G>A MANE Select	NP_001004439.1:p.Ala445Thr