Canonical Allele Identifier: CA2184934324
Gene: ITGA11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68335726T= , CM000677.2:g.68335726T= GRCh38
NC_000015.9:g.68628064T= , CM000677.1:g.68628064T= GRCh37
NC_000015.8:g.66415118T= NCBI36
NG_046911.1:g.101435A=

Transcript Alleles

HGVS Amino-acid change
ENST00000315757.9:c.1396A= MANE Select ENSP00000327290.7:p.Thr466=
ENST00000315757.8:c.1396A= ENSP00000327290.7:p.Thr466=
ENST00000423218.6:c.1396A= ENSP00000403392.2:p.Thr466=
ENST00000566429.1:n.285A=
ENST00000569346.5:n.375A=
NM_001004439.1:c.1396A= NP_001004439.1:p.Thr466=
XM_005254228.2:c.1090A= XP_005254285.1:p.Thr364=
XM_011521363.1:c.1189A= XP_011519665.1:p.Thr397=
XM_005254228.3:c.1090A= XP_005254285.1:p.Thr364=
XM_011521363.2:c.1189A= XP_011519665.1:p.Thr397=
NM_001004439.2:c.1396A= MANE Select NP_001004439.1:p.Thr466=