Canonical Allele Identifier: CA618703905

Gene: ITGA11

Linked Data

• dbSNP Id: rs1177658558
• gnomAD v2: 15-68628082-G-GAA
• gnomAD v4: 15-68335744-G-GAA
• MyVariant Identifiers: chr15:g.68628082_68628083insAA (hg19) ; chr15:g.68335744_68335745insAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335744_68335745insAA , CM000677.2:g.68335744_68335745insAA	GRCh38
NC_000015.9:g.68628082_68628083insAA , CM000677.1:g.68628082_68628083insAA	GRCh37
NC_000015.8:g.66415136_66415137insAA	NCBI36
NG_046911.1:g.101416_101417insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1377_1378insTT MANE Select	ENSP00000327290.7:p.His460PhefsTer18
ENST00000315757.8:c.1377_1378insTT	ENSP00000327290.7:p.His460PhefsTer18
ENST00000423218.6:c.1377_1378insTT	ENSP00000403392.2:p.His460PhefsTer18
ENST00000566429.1:n.266_267insTT
ENST00000569346.5:n.356_357insTT
NM_001004439.1:c.1377_1378insTT	NP_001004439.1:p.His460PhefsTer18
XM_005254228.2:c.1071_1072insTT	XP_005254285.1:p.His358PhefsTer18
XM_011521363.1:c.1170_1171insTT	XP_011519665.1:p.His391PhefsTer18
XM_005254228.3:c.1071_1072insTT	XP_005254285.1:p.His358PhefsTer18
XM_011521363.2:c.1170_1171insTT	XP_011519665.1:p.His391PhefsTer18
NM_001004439.2:c.1377_1378insTT MANE Select	NP_001004439.1:p.His460PhefsTer18