Canonical Allele Identifier: CA1865974893

Gene: HSD17B3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96235568C= , CM000671.2:g.96235568C=	GRCh38
NC_000009.11:g.98997850C= , CM000671.1:g.98997850C=	GRCh37
NC_000009.10:g.98037671C=	NCBI36
NG_008157.1:g.71585G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.675G=	ENSP00000364411.2:p.Ala225=
ENST00000375263.8:c.825G= MANE Select	ENSP00000364412.3:p.Ala275=
ENST00000463517.2:n.2367G=
ENST00000464104.6:n.1763G=
ENST00000467499.6:c.*524G=	ENSP00000498077.1:n.*524G=
ENST00000494814.6:n.375G=
ENST00000643789.1:c.3117G=
ENST00000648146.1:c.963G=	ENSP00000497238.1:n.963G=
ENST00000648332.1:c.502G=	ENSP00000497562.1:n.502G=
ENST00000648799.1:c.717G=	ENSP00000498039.1:p.Ala239=
ENST00000650005.1:c.754G=	ENSP00000498121.1:n.754G=
ENST00000375262.3:c.675G=	ENSP00000364411.2:p.Ala225=
ENST00000375263.7:c.825G=	ENSP00000364412.3:p.Ala275=
ENST00000464104.5:n.678G=
ENST00000467499.5:n.85G=
ENST00000494814.5:n.384G=
NM_000197.1:c.825G=	NP_000188.1:p.Ala275=
XM_005251970.3:c.465G=	XP_005252027.1:p.Ala155=
XM_011518618.1:c.825G=	XP_011516920.1:p.Ala275=
XM_011518619.1:c.825G=	XP_011516921.1:p.Ala275=
XM_011518620.1:c.717G=	XP_011516922.1:p.Ala239=
NM_000197.2:c.825G= MANE Select	NP_000188.1:p.Ala275=
XM_011518618.2:c.825G=	XP_011516920.1:p.Ala275=
XM_011518619.2:c.825G=	XP_011516921.1:p.Ala275=
XM_017014671.1:c.825G=	XP_016870160.1:p.Ala275=
XM_017014672.1:c.825G=	XP_016870161.1:p.Ala275=
XM_017014673.2:c.789G=	XP_016870162.1:p.Ala263=
XM_017014674.1:c.717G=	XP_016870163.1:p.Ala239=
XM_017014675.1:c.663G=	XP_016870164.1:p.Ala221=
XM_017014677.1:c.465G=	XP_016870166.1:p.Ala155=
XM_024447529.1:c.663G=	XP_024303297.1:p.Ala221=
XR_002956778.1:n.3297G=