Canonical Allele Identifier: CA1865974971

Gene: HSD17B3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96235627C= , CM000671.2:g.96235627C=	GRCh38
NC_000009.11:g.98997909C= , CM000671.1:g.98997909C=	GRCh37
NC_000009.10:g.98037730C=	NCBI36
NG_008157.1:g.71526G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.673-57G=	ENSP00000364411.2:n.673-57G=
ENST00000375263.8:c.823-57G= MANE Select	ENSP00000364412.3:n.823-57G=
ENST00000463517.2:n.2365-57G=
ENST00000464104.6:n.1761-57G=
ENST00000467499.6:c.*522-57G=	ENSP00000498077.1:n.*522-57G=
ENST00000494814.6:n.373-57G=
ENST00000643789.1:c.3115-57G=
ENST00000648146.1:c.961-57G=	ENSP00000497238.1:n.961-57G=
ENST00000648332.1:c.500-57G=	ENSP00000497562.1:n.500-57G=
ENST00000648799.1:c.715-57G=	ENSP00000498039.1:n.715-57G=
ENST00000650005.1:c.752-57G=	ENSP00000498121.1:n.752-57G=
ENST00000375262.3:c.673-57G=	ENSP00000364411.2:n.673-57G=
ENST00000375263.7:c.823-57G=	ENSP00000364412.3:n.823-57G=
ENST00000464104.5:n.676-57G=
ENST00000467499.5:n.83-57G=
ENST00000494814.5:n.382-57G=
NM_000197.1:c.823-57G=	NP_000188.1:n.823-57G=
XM_005251970.3:c.463-57G=	XP_005252027.1:n.463-57G=
XM_011518618.1:c.823-57G=	XP_011516920.1:n.823-57G=
XM_011518619.1:c.823-57G=	XP_011516921.1:n.823-57G=
XM_011518620.1:c.715-57G=	XP_011516922.1:n.715-57G=
NM_000197.2:c.823-57G= MANE Select	NP_000188.1:n.823-57G=
XM_011518618.2:c.823-57G=	XP_011516920.1:n.823-57G=
XM_011518619.2:c.823-57G=	XP_011516921.1:n.823-57G=
XM_017014671.1:c.823-57G=	XP_016870160.1:n.823-57G=
XM_017014672.1:c.823-57G=	XP_016870161.1:n.823-57G=
XM_017014673.2:c.787-57G=	XP_016870162.1:n.787-57G=
XM_017014674.1:c.715-57G=	XP_016870163.1:n.715-57G=
XM_017014675.1:c.661-57G=	XP_016870164.1:n.661-57G=
XM_017014677.1:c.463-57G=	XP_016870166.1:n.463-57G=
XM_024447529.1:c.661-57G=	XP_024303297.1:n.661-57G=
XR_002956778.1:n.3295-57G=