Canonical Allele Identifier: CA971061853

Gene: ITGA11

Linked Data

• dbSNP Id: rs1894321724
• gnomAD v3: 15-68335588-G-GCA
• gnomAD v4: 15-68335588-G-GCA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335589_68335590insAC , CM000677.2:g.68335589_68335590insAC	GRCh38
NC_000015.9:g.68627927_68627928insAC , CM000677.1:g.68627927_68627928insAC	GRCh37
NC_000015.8:g.66414981_66414982insAC	NCBI36
NG_046911.1:g.101572_101573insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1425+108_1425+109insTG MANE Select	ENSP00000327290.7:n.1425+108_1425+109insTG
ENST00000315757.8:c.1425+108_1425+109insTG	ENSP00000327290.7:n.1425+108_1425+109insTG
ENST00000423218.6:c.1425+108_1425+109insTG	ENSP00000403392.2:n.1425+108_1425+109insTG
ENST00000566429.1:n.314+108_314+109insTG
ENST00000569346.5:n.404+108_404+109insTG
NM_001004439.1:c.1425+108_1425+109insTG	NP_001004439.1:n.1425+108_1425+109insTG
XM_005254228.2:c.1119+108_1119+109insTG	XP_005254285.1:n.1119+108_1119+109insTG
XM_011521363.1:c.1218+108_1218+109insTG	XP_011519665.1:n.1218+108_1218+109insTG
XM_005254228.3:c.1119+108_1119+109insTG	XP_005254285.1:n.1119+108_1119+109insTG
XM_011521363.2:c.1218+108_1218+109insTG	XP_011519665.1:n.1218+108_1218+109insTG
NM_001004439.2:c.1425+108_1425+109insTG MANE Select	NP_001004439.1:n.1425+108_1425+109insTG