Canonical Allele Identifier: CA2184934342

Gene: ITGA11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335758_68335759delinsAT , CM000677.2:g.68335758_68335759delinsAT	GRCh38
NC_000015.9:g.68628096_68628097delinsAT , CM000677.1:g.68628096_68628097delinsAT	GRCh37
NC_000015.8:g.66415150_66415151delinsAT	NCBI36
NG_046911.1:g.101402_101403delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1363_1364delinsAT MANE Select	ENSP00000327290.7:p.Ile455=
ENST00000315757.8:c.1363_1364delinsAT	ENSP00000327290.7:p.Ile455=
ENST00000423218.6:c.1363_1364delinsAT	ENSP00000403392.2:p.Ile455=
ENST00000566429.1:n.252_253delinsAT
ENST00000569346.5:n.342_343delinsAT
NM_001004439.1:c.1363_1364delinsAT	NP_001004439.1:p.Ile455=
XM_005254228.2:c.1057_1058delinsAT	XP_005254285.1:p.Ile353=
XM_011521363.1:c.1156_1157delinsAT	XP_011519665.1:p.Ile386=
XM_005254228.3:c.1057_1058delinsAT	XP_005254285.1:p.Ile353=
XM_011521363.2:c.1156_1157delinsAT	XP_011519665.1:p.Ile386=
NM_001004439.2:c.1363_1364delinsAT MANE Select	NP_001004439.1:p.Ile455=