Canonical Allele Identifier: CA1865974680

Gene: HSD17B3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96235487G= , CM000671.2:g.96235487G=	GRCh38
NC_000009.11:g.98997769G= , CM000671.1:g.98997769G=	GRCh37
NC_000009.10:g.98037590G=	NCBI36
NG_008157.1:g.71666C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.756C=	ENSP00000364411.2:p.Tyr252=
ENST00000375263.8:c.906C= MANE Select	ENSP00000364412.3:p.Tyr302=
ENST00000463517.2:n.2448C=
ENST00000464104.6:n.1844C=
ENST00000467499.6:c.*605C=	ENSP00000498077.1:n.*605C=
ENST00000494814.6:n.456C=
ENST00000643789.1:c.3198C=
ENST00000648146.1:c.1044C=	ENSP00000497238.1:n.1044C=
ENST00000648332.1:c.583C=	ENSP00000497562.1:n.583C=
ENST00000650005.1:c.835C=	ENSP00000498121.1:n.835C=
ENST00000375262.3:c.756C=	ENSP00000364411.2:p.Tyr252=
ENST00000375263.7:c.906C=	ENSP00000364412.3:p.Tyr302=
ENST00000464104.5:n.759C=
ENST00000467499.5:n.166C=
ENST00000494814.5:n.465C=
NM_000197.1:c.906C=	NP_000188.1:p.Tyr302=
XM_005251970.3:c.546C=	XP_005252027.1:p.Tyr182=
XM_011518618.1:c.906C=	XP_011516920.1:p.Tyr302=
XM_011518619.1:c.906C=	XP_011516921.1:p.Tyr302=
XM_011518620.1:c.798C=	XP_011516922.1:p.Tyr266=
NM_000197.2:c.906C= MANE Select	NP_000188.1:p.Tyr302=
XM_011518618.2:c.906C=	XP_011516920.1:p.Tyr302=
XM_011518619.2:c.906C=	XP_011516921.1:p.Tyr302=
XM_017014671.1:c.906C=	XP_016870160.1:p.Tyr302=
XM_017014672.1:c.906C=	XP_016870161.1:p.Tyr302=
XM_017014673.2:c.870C=	XP_016870162.1:p.Tyr290=
XM_017014674.1:c.798C=	XP_016870163.1:p.Tyr266=
XM_017014675.1:c.744C=	XP_016870164.1:p.Tyr248=
XM_017014677.1:c.546C=	XP_016870166.1:p.Tyr182=
XM_024447529.1:c.744C=	XP_024303297.1:p.Tyr248=
XR_002956778.1:n.3378C=