Canonical Allele Identifier: CA2629178603

Gene: ITGA11

Linked Data

• gnomAD v4: 15-68335584-GACTGCCCTTTGGGGCACCCAGTGGTCCAGGCATGCCTGTATTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335593_68335635del , CM000677.2:g.68335593_68335635del	GRCh38
NC_000015.9:g.68627931_68627973del , CM000677.1:g.68627931_68627973del	GRCh37
NC_000015.8:g.66414985_66415027del	NCBI36
NG_046911.1:g.101534_101576del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1425+70_1425+112del MANE Select	ENSP00000327290.7:n.1425+70_1425+112del
ENST00000315757.8:c.1425+70_1425+112del	ENSP00000327290.7:n.1425+70_1425+112del
ENST00000423218.6:c.1425+70_1425+112del	ENSP00000403392.2:n.1425+70_1425+112del
ENST00000566429.1:n.314+70_314+112del
ENST00000569346.5:n.404+70_404+112del
NM_001004439.1:c.1425+70_1425+112del	NP_001004439.1:n.1425+70_1425+112del
XM_005254228.2:c.1119+70_1119+112del	XP_005254285.1:n.1119+70_1119+112del
XM_011521363.1:c.1218+70_1218+112del	XP_011519665.1:n.1218+70_1218+112del
XM_005254228.3:c.1119+70_1119+112del	XP_005254285.1:n.1119+70_1119+112del
XM_011521363.2:c.1218+70_1218+112del	XP_011519665.1:n.1218+70_1218+112del
NM_001004439.2:c.1425+70_1425+112del MANE Select	NP_001004439.1:n.1425+70_1425+112del