Canonical Allele Identifier: CA2804596028

Gene: ITGA11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335832_68335836dup , CM000677.2:g.68335832_68335836dup	GRCh38
NC_000015.9:g.68628170_68628174dup , CM000677.1:g.68628170_68628174dup	GRCh37
NC_000015.8:g.66415224_66415228dup	NCBI36
NG_046911.1:g.101327_101331dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1288_1292dup MANE Select	ENSP00000327290.7:p.Val432HisfsTer?
ENST00000315757.8:c.1288_1292dup	ENSP00000327290.7:p.Val432HisfsTer?
ENST00000423218.6:c.1288_1292dup	ENSP00000403392.2:p.Val432HisfsTer?
ENST00000566429.1:n.197-20_197-16dup
ENST00000569346.5:n.267_271dup
NM_001004439.1:c.1288_1292dup	NP_001004439.1:p.Val432HisfsTer?
XM_005254228.2:c.982_986dup	XP_005254285.1:p.Val330HisfsTer?
XM_011521363.1:c.1081_1085dup	XP_011519665.1:p.Val363HisfsTer?
XM_005254228.3:c.982_986dup	XP_005254285.1:p.Val330HisfsTer?
XM_011521363.2:c.1081_1085dup	XP_011519665.1:p.Val363HisfsTer?
NM_001004439.2:c.1288_1292dup MANE Select	NP_001004439.1:p.Val432HisfsTer?