Canonical Allele Identifier: CA2690815779
Gene: HSD17B3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.96235328del , CM000671.2:g.96235328del GRCh38
NC_000009.11:g.98997610del , CM000671.1:g.98997610del GRCh37
NC_000009.10:g.98037431del NCBI36
NG_008157.1:g.71826del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375263.8:c.*133del MANE Select ENSP00000364412.3:n.*133del
ENST00000467499.6:c.*765del ENSP00000498077.1:n.*765del
ENST00000494814.6:n.616del
ENST00000375262.3:c.*133del ENSP00000364411.2:n.*133del
ENST00000375263.7:c.*133del ENSP00000364412.3:n.*133del
ENST00000464104.5:n.919del
ENST00000467499.5:n.326del
ENST00000494814.5:n.625del
NM_000197.1:c.*133del NP_000188.1:n.*133del
XM_005251970.3:c.*133del XP_005252027.1:n.*133del
XM_011518618.1:c.*133del XP_011516920.1:n.*133del
XM_011518619.1:c.*133del XP_011516921.1:n.*133del
XM_011518620.1:c.*133del XP_011516922.1:n.*133del
NM_000197.2:c.*133del MANE Select NP_000188.1:n.*133del
XM_011518618.2:c.*133del XP_011516920.1:n.*133del
XM_011518619.2:c.*133del XP_011516921.1:n.*133del
XM_017014671.1:c.*133del XP_016870160.1:n.*133del
XM_017014672.1:c.*133del XP_016870161.1:n.*133del
XM_017014673.2:c.*133del XP_016870162.1:n.*133del
XM_017014674.1:c.*133del XP_016870163.1:n.*133del
XM_017014675.1:c.*133del XP_016870164.1:n.*133del
XM_017014677.1:c.*133del XP_016870166.1:n.*133del
XM_024447529.1:c.*133del XP_024303297.1:n.*133del
XR_002956778.1:n.3538del