Canonical Allele Identifier: CA2838239853

Gene: ITGA11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335341_68335342del , CM000677.2:g.68335341_68335342del	GRCh38
NC_000015.9:g.68627679_68627680del , CM000677.1:g.68627679_68627680del	GRCh37
NC_000015.8:g.66414733_66414734del	NCBI36
NG_046911.1:g.101820_101821del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1425+356_1425+357del MANE Select	ENSP00000327290.7:n.1425+356_1425+357del
ENST00000315757.8:c.1425+356_1425+357del	ENSP00000327290.7:n.1425+356_1425+357del
ENST00000423218.6:c.1425+356_1425+357del	ENSP00000403392.2:n.1425+356_1425+357del
ENST00000566429.1:n.314+356_314+357del
ENST00000569346.5:n.404+356_404+357del
NM_001004439.1:c.1425+356_1425+357del	NP_001004439.1:n.1425+356_1425+357del
XM_005254228.2:c.1119+356_1119+357del	XP_005254285.1:n.1119+356_1119+357del
XM_011521363.1:c.1218+356_1218+357del	XP_011519665.1:n.1218+356_1218+357del
XM_005254228.3:c.1119+356_1119+357del	XP_005254285.1:n.1119+356_1119+357del
XM_011521363.2:c.1218+356_1218+357del	XP_011519665.1:n.1218+356_1218+357del
NM_001004439.2:c.1425+356_1425+357del MANE Select	NP_001004439.1:n.1425+356_1425+357del