Canonical Allele Identifier: CA1865974958

Gene: HSD17B3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96235609A= , CM000671.2:g.96235609A=	GRCh38
NC_000009.11:g.98997891A= , CM000671.1:g.98997891A=	GRCh37
NC_000009.10:g.98037712A=	NCBI36
NG_008157.1:g.71544T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.673-39T=	ENSP00000364411.2:n.673-39T=
ENST00000375263.8:c.823-39T= MANE Select	ENSP00000364412.3:n.823-39T=
ENST00000463517.2:n.2365-39T=
ENST00000464104.6:n.1761-39T=
ENST00000467499.6:c.*522-39T=	ENSP00000498077.1:n.*522-39T=
ENST00000494814.6:n.373-39T=
ENST00000643789.1:c.3115-39T=
ENST00000648146.1:c.961-39T=	ENSP00000497238.1:n.961-39T=
ENST00000648332.1:c.500-39T=	ENSP00000497562.1:n.500-39T=
ENST00000648799.1:c.715-39T=	ENSP00000498039.1:n.715-39T=
ENST00000650005.1:c.752-39T=	ENSP00000498121.1:n.752-39T=
ENST00000375262.3:c.673-39T=	ENSP00000364411.2:n.673-39T=
ENST00000375263.7:c.823-39T=	ENSP00000364412.3:n.823-39T=
ENST00000464104.5:n.676-39T=
ENST00000467499.5:n.83-39T=
ENST00000494814.5:n.382-39T=
NM_000197.1:c.823-39T=	NP_000188.1:n.823-39T=
XM_005251970.3:c.463-39T=	XP_005252027.1:n.463-39T=
XM_011518618.1:c.823-39T=	XP_011516920.1:n.823-39T=
XM_011518619.1:c.823-39T=	XP_011516921.1:n.823-39T=
XM_011518620.1:c.715-39T=	XP_011516922.1:n.715-39T=
NM_000197.2:c.823-39T= MANE Select	NP_000188.1:n.823-39T=
XM_011518618.2:c.823-39T=	XP_011516920.1:n.823-39T=
XM_011518619.2:c.823-39T=	XP_011516921.1:n.823-39T=
XM_017014671.1:c.823-39T=	XP_016870160.1:n.823-39T=
XM_017014672.1:c.823-39T=	XP_016870161.1:n.823-39T=
XM_017014673.2:c.787-39T=	XP_016870162.1:n.787-39T=
XM_017014674.1:c.715-39T=	XP_016870163.1:n.715-39T=
XM_017014675.1:c.661-39T=	XP_016870164.1:n.661-39T=
XM_017014677.1:c.463-39T=	XP_016870166.1:n.463-39T=
XM_024447529.1:c.661-39T=	XP_024303297.1:n.661-39T=
XR_002956778.1:n.3295-39T=