Canonical Allele Identifier: CA2838239860

Gene: ITGA11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335800dup , CM000677.2:g.68335800dup	GRCh38
NC_000015.9:g.68628138dup , CM000677.1:g.68628138dup	GRCh37
NC_000015.8:g.66415192dup	NCBI36
NG_046911.1:g.101361dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1322dup MANE Select	ENSP00000327290.7:p.Tyr441Ter
ENST00000315757.8:c.1322dup	ENSP00000327290.7:p.Tyr441Ter
ENST00000423218.6:c.1322dup	ENSP00000403392.2:p.Tyr441Ter
ENST00000566429.1:n.211dup
ENST00000569346.5:n.301dup
NM_001004439.1:c.1322dup	NP_001004439.1:p.Tyr441Ter
XM_005254228.2:c.1016dup	XP_005254285.1:p.Tyr339Ter
XM_011521363.1:c.1115dup	XP_011519665.1:p.Tyr372Ter
XM_005254228.3:c.1016dup	XP_005254285.1:p.Tyr339Ter
XM_011521363.2:c.1115dup	XP_011519665.1:p.Tyr372Ter
NM_001004439.2:c.1322dup MANE Select	NP_001004439.1:p.Tyr441Ter