Canonical Allele Identifier: CA2184934327
Gene: ITGA11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68335734C= , CM000677.2:g.68335734C= GRCh38
NC_000015.9:g.68628072C= , CM000677.1:g.68628072C= GRCh37
NC_000015.8:g.66415126C= NCBI36
NG_046911.1:g.101427G=

Transcript Alleles

HGVS Amino-acid change
ENST00000315757.9:c.1388G= MANE Select ENSP00000327290.7:p.Arg463=
ENST00000315757.8:c.1388G= ENSP00000327290.7:p.Arg463=
ENST00000423218.6:c.1388G= ENSP00000403392.2:p.Arg463=
ENST00000566429.1:n.277G=
ENST00000569346.5:n.367G=
NM_001004439.1:c.1388G= NP_001004439.1:p.Arg463=
XM_005254228.2:c.1082G= XP_005254285.1:p.Arg361=
XM_011521363.1:c.1181G= XP_011519665.1:p.Arg394=
XM_005254228.3:c.1082G= XP_005254285.1:p.Arg361=
XM_011521363.2:c.1181G= XP_011519665.1:p.Arg394=
NM_001004439.2:c.1388G= MANE Select NP_001004439.1:p.Arg463=