Canonical Allele Identifier: CA2184934335

Gene: ITGA11

Linked Data

• dbSNP Id: rs1894331889

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335746_68335747insCAGGAACAGGATGTTCTG , CM000677.2:g.68335746_68335747insCAGGAACAGGATGTTCTG	GRCh38
NC_000015.9:g.68628084_68628085insCAGGAACAGGATGTTCTG , CM000677.1:g.68628084_68628085insCAGGAACAGGATGTTCTG	GRCh37
NC_000015.8:g.66415138_66415139insCAGGAACAGGATGTTCTG	NCBI36
NG_046911.1:g.101414_101415insCAGAACATCCTGTTCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1375_1376insCAGAACATCCTGTTCCTG MANE Select	ENSP00000327290.7:p.Met459delinsThrGluHisProValProVal
ENST00000315757.8:c.1375_1376insCAGAACATCCTGTTCCTG	ENSP00000327290.7:p.Met459delinsThrGluHisProValProVal
ENST00000423218.6:c.1375_1376insCAGAACATCCTGTTCCTG	ENSP00000403392.2:p.Met459delinsThrGluHisProValProVal
ENST00000566429.1:n.264_265insCAGAACATCCTGTTCCTG
ENST00000569346.5:n.354_355insCAGAACATCCTGTTCCTG
NM_001004439.1:c.1375_1376insCAGAACATCCTGTTCCTG	NP_001004439.1:p.Met459delinsThrGluHisProValProVal
XM_005254228.2:c.1069_1070insCAGAACATCCTGTTCCTG	XP_005254285.1:p.Met357delinsThrGluHisProValProVal
XM_011521363.1:c.1168_1169insCAGAACATCCTGTTCCTG	XP_011519665.1:p.Met390delinsThrGluHisProValProVal
XM_005254228.3:c.1069_1070insCAGAACATCCTGTTCCTG	XP_005254285.1:p.Met357delinsThrGluHisProValProVal
XM_011521363.2:c.1168_1169insCAGAACATCCTGTTCCTG	XP_011519665.1:p.Met390delinsThrGluHisProValProVal
NM_001004439.2:c.1375_1376insCAGAACATCCTGTTCCTG MANE Select	NP_001004439.1:p.Met459delinsThrGluHisProValProVal