Canonical Allele Identifier: CA2575772202

Gene: ITGA11

Linked Data

• gnomAD v4: 15-68335782-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335788del , CM000677.2:g.68335788del	GRCh38
NC_000015.9:g.68628126del , CM000677.1:g.68628126del	GRCh37
NC_000015.8:g.66415180del	NCBI36
NG_046911.1:g.101378del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1339del MANE Select	ENSP00000327290.7:p.Arg447GlyfsTer30
ENST00000315757.8:c.1339del	ENSP00000327290.7:p.Arg447GlyfsTer30
ENST00000423218.6:c.1339del	ENSP00000403392.2:p.Arg447GlyfsTer30
ENST00000566429.1:n.228del
ENST00000569346.5:n.318del
NM_001004439.1:c.1339del	NP_001004439.1:p.Arg447GlyfsTer30
XM_005254228.2:c.1033del	XP_005254285.1:p.Arg345GlyfsTer30
XM_011521363.1:c.1132del	XP_011519665.1:p.Arg378GlyfsTer30
XM_005254228.3:c.1033del	XP_005254285.1:p.Arg345GlyfsTer30
XM_011521363.2:c.1132del	XP_011519665.1:p.Arg378GlyfsTer30
NM_001004439.2:c.1339del MANE Select	NP_001004439.1:p.Arg447GlyfsTer30