Canonical Allele Identifier: CA383140175
Community Standard Title: NM_152722.5(HEPACAM):c.789G>A (p.Trp263Ter)
Gene: HEPACAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.124923354C>T , CM000673.2:g.124923354C>T GRCh38
NC_000011.9:g.124793250C>T , CM000673.1:g.124793250C>T GRCh37
NC_000011.8:g.124298460C>T NCBI36
NG_029603.1:g.18059G>A

Transcript Alleles

HGVS Amino-acid Change
NM_152722.5:c.789G>A MANE Select NP_689935.2:p.Trp263Ter
ENST00000298251.5:c.789G>A MANE Select ENSP00000298251.4:p.Trp263Ter
NM_152722.4:c.789G>A NP_689935.2:p.Trp263Ter
ENST00000298251.4:c.789G>A ENSP00000298251.4:p.Trp263Ter
ENST00000703807.1:c.789G>A ENSP00000515485.1:p.Trp263Ter
XM_005271449.1:c.789G>A XP_005271506.1:p.Trp263Ter
XM_005271449.2:c.789G>A XP_005271506.1:p.Trp263Ter
XM_006718786.1:c.789G>A XP_006718849.1:p.Trp263Ter
XM_011542669.1:c.789G>A XP_011540971.1:p.Trp263Ter
XM_017017361.1:c.789G>A XP_016872850.1:p.Trp263Ter
XR_001748429.2:n.325-20046C>T