Canonical Allele Identifier: CA971061839

Gene: ITGA11

Linked Data

• dbSNP Id: rs1894321330
• gnomAD v3: 15-68335584-G-GGTCCAGGC
• gnomAD v4: 15-68335584-G-GGTCCAGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335584_68335585insGTCCAGGC , CM000677.2:g.68335584_68335585insGTCCAGGC	GRCh38
NC_000015.9:g.68627922_68627923insGTCCAGGC , CM000677.1:g.68627922_68627923insGTCCAGGC	GRCh37
NC_000015.8:g.66414976_66414977insGTCCAGGC	NCBI36
NG_046911.1:g.101576_101577insGCCTGGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1425+112_1425+113insGCCTGGAC MANE Select	ENSP00000327290.7:n.1425+112_1425+113insGCCTGGAC
ENST00000315757.8:c.1425+112_1425+113insGCCTGGAC	ENSP00000327290.7:n.1425+112_1425+113insGCCTGGAC
ENST00000423218.6:c.1425+112_1425+113insGCCTGGAC	ENSP00000403392.2:n.1425+112_1425+113insGCCTGGAC
ENST00000566429.1:n.314+112_314+113insGCCTGGAC
ENST00000569346.5:n.404+112_404+113insGCCTGGAC
NM_001004439.1:c.1425+112_1425+113insGCCTGGAC	NP_001004439.1:n.1425+112_1425+113insGCCTGGAC
XM_005254228.2:c.1119+112_1119+113insGCCTGGAC	XP_005254285.1:n.1119+112_1119+113insGCCTGGAC
XM_011521363.1:c.1218+112_1218+113insGCCTGGAC	XP_011519665.1:n.1218+112_1218+113insGCCTGGAC
XM_005254228.3:c.1119+112_1119+113insGCCTGGAC	XP_005254285.1:n.1119+112_1119+113insGCCTGGAC
XM_011521363.2:c.1218+112_1218+113insGCCTGGAC	XP_011519665.1:n.1218+112_1218+113insGCCTGGAC
NM_001004439.2:c.1425+112_1425+113insGCCTGGAC MANE Select	NP_001004439.1:n.1425+112_1425+113insGCCTGGAC