Canonical Allele Identifier: CA2184934233
Gene: ITGA11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68335541A= , CM000677.2:g.68335541A= GRCh38
NC_000015.9:g.68627879A= , CM000677.1:g.68627879A= GRCh37
NC_000015.8:g.66414933A= NCBI36
NG_046911.1:g.101620T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000315757.9:c.1425+156T= MANE Select ENSP00000327290.7:n.1425+156T=
ENST00000315757.8:c.1425+156T= ENSP00000327290.7:n.1425+156T=
ENST00000423218.6:c.1425+156T= ENSP00000403392.2:n.1425+156T=
ENST00000566429.1:n.314+156T=
ENST00000569346.5:n.404+156T=
NM_001004439.1:c.1425+156T= NP_001004439.1:n.1425+156T=
XM_005254228.2:c.1119+156T= XP_005254285.1:n.1119+156T=
XM_011521363.1:c.1218+156T= XP_011519665.1:n.1218+156T=
XM_005254228.3:c.1119+156T= XP_005254285.1:n.1119+156T=
XM_011521363.2:c.1218+156T= XP_011519665.1:n.1218+156T=
NM_001004439.2:c.1425+156T= MANE Select NP_001004439.1:n.1425+156T=
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