Canonical Allele Identifier: CA618703891

Gene: ITGA11

Linked Data

• dbSNP Id: rs1181319860
• gnomAD v2: 15-68628008-C-T
• gnomAD v4: 15-68335670-C-T
• MyVariant Identifiers: chr15:g.68628008C>T (hg19) ; chr15:g.68335670C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335670C>T , CM000677.2:g.68335670C>T	GRCh38
NC_000015.9:g.68628008C>T , CM000677.1:g.68628008C>T	GRCh37
NC_000015.8:g.66415062C>T	NCBI36
NG_046911.1:g.101491G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1425+27G>A MANE Select	ENSP00000327290.7:n.1425+27G>A
ENST00000315757.8:c.1425+27G>A	ENSP00000327290.7:n.1425+27G>A
ENST00000423218.6:c.1425+27G>A	ENSP00000403392.2:n.1425+27G>A
ENST00000566429.1:n.314+27G>A
ENST00000569346.5:n.404+27G>A
NM_001004439.1:c.1425+27G>A	NP_001004439.1:n.1425+27G>A
XM_005254228.2:c.1119+27G>A	XP_005254285.1:n.1119+27G>A
XM_011521363.1:c.1218+27G>A	XP_011519665.1:n.1218+27G>A
XM_005254228.3:c.1119+27G>A	XP_005254285.1:n.1119+27G>A
XM_011521363.2:c.1218+27G>A	XP_011519665.1:n.1218+27G>A
NM_001004439.2:c.1425+27G>A MANE Select	NP_001004439.1:n.1425+27G>A