Canonical Allele Identifier: CA2804596027

Gene: ITGA11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335787_68335788dup , CM000677.2:g.68335787_68335788dup	GRCh38
NC_000015.9:g.68628125_68628126dup , CM000677.1:g.68628125_68628126dup	GRCh37
NC_000015.8:g.66415179_66415180dup	NCBI36
NG_046911.1:g.101377_101378dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1338_1339dup MANE Select	ENSP00000327290.7:p.Arg447ProfsTer31
ENST00000315757.8:c.1338_1339dup	ENSP00000327290.7:p.Arg447ProfsTer31
ENST00000423218.6:c.1338_1339dup	ENSP00000403392.2:p.Arg447ProfsTer31
ENST00000566429.1:n.227_228dup
ENST00000569346.5:n.317_318dup
NM_001004439.1:c.1338_1339dup	NP_001004439.1:p.Arg447ProfsTer31
XM_005254228.2:c.1032_1033dup	XP_005254285.1:p.Arg345ProfsTer31
XM_011521363.1:c.1131_1132dup	XP_011519665.1:p.Arg378ProfsTer31
XM_005254228.3:c.1032_1033dup	XP_005254285.1:p.Arg345ProfsTer31
XM_011521363.2:c.1131_1132dup	XP_011519665.1:p.Arg378ProfsTer31
NM_001004439.2:c.1338_1339dup MANE Select	NP_001004439.1:p.Arg447ProfsTer31