Canonical Allele Identifier: CA1865974646
Gene: HSD17B3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.96235470T= , CM000671.2:g.96235470T= GRCh38
NC_000009.11:g.98997752T= , CM000671.1:g.98997752T= GRCh37
NC_000009.10:g.98037573T= NCBI36
NG_008157.1:g.71683A=

Transcript Alleles

HGVS Amino-acid change
ENST00000375262.4:c.773A= ENSP00000364411.2:p.Lys258=
ENST00000375263.8:c.923A= MANE Select ENSP00000364412.3:p.Lys308=
ENST00000463517.2:n.2465A=
ENST00000464104.6:n.1861A=
ENST00000467499.6:c.*622A= ENSP00000498077.1:n.*622A=
ENST00000494814.6:n.473A=
ENST00000643789.1:c.3215A=
ENST00000648146.1:c.1061A= ENSP00000497238.1:n.1061A=
ENST00000648332.1:c.600A= ENSP00000497562.1:n.600A=
ENST00000650005.1:c.852A= ENSP00000498121.1:n.852A=
ENST00000375262.3:c.773A= ENSP00000364411.2:p.Lys258=
ENST00000375263.7:c.923A= ENSP00000364412.3:p.Lys308=
ENST00000464104.5:n.776A=
ENST00000467499.5:n.183A=
ENST00000494814.5:n.482A=
NM_000197.1:c.923A= NP_000188.1:p.Lys308=
XM_005251970.3:c.563A= XP_005252027.1:p.Lys188=
XM_011518618.1:c.923A= XP_011516920.1:p.Lys308=
XM_011518619.1:c.923A= XP_011516921.1:p.Lys308=
XM_011518620.1:c.815A= XP_011516922.1:p.Lys272=
NM_000197.2:c.923A= MANE Select NP_000188.1:p.Lys308=
XM_011518618.2:c.923A= XP_011516920.1:p.Lys308=
XM_011518619.2:c.923A= XP_011516921.1:p.Lys308=
XM_017014671.1:c.923A= XP_016870160.1:p.Lys308=
XM_017014672.1:c.923A= XP_016870161.1:p.Lys308=
XM_017014673.2:c.887A= XP_016870162.1:p.Lys296=
XM_017014674.1:c.815A= XP_016870163.1:p.Lys272=
XM_017014675.1:c.761A= XP_016870164.1:p.Lys254=
XM_017014677.1:c.563A= XP_016870166.1:p.Lys188=
XM_024447529.1:c.761A= XP_024303297.1:p.Lys254=
XR_002956778.1:n.3395A=