Canonical Allele Identifier: CA1865972867

Gene: HSD17B3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96298429G= , CM000671.2:g.96298429G=	GRCh38
NC_000009.11:g.99060711G= , CM000671.1:g.99060711G=	GRCh37
NC_000009.10:g.98100532G=	NCBI36
NG_008157.1:g.8724C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375262.4:c.188C=	ENSP00000364411.2:p.Ala63=
ENST00000375263.8:c.188C= MANE Select	ENSP00000364412.3:p.Ala63=
ENST00000463517.2:n.997C=
ENST00000464104.6:n.658C=
ENST00000467499.6:c.188C=	ENSP00000498077.1:p.Ala63=
ENST00000643789.1:c.2480C=
ENST00000648146.1:c.188C=	ENSP00000497238.1:p.Ala63=
ENST00000648332.1:c.188C=	ENSP00000497562.1:p.Ala63=
ENST00000648799.1:c.188C=	ENSP00000498039.1:p.Ala63=
ENST00000650005.1:c.188C=	ENSP00000498121.1:p.Ala63=
ENST00000650386.1:c.188C=	ENSP00000497464.1:p.Ala63=
ENST00000375262.3:c.188C=	ENSP00000364411.2:p.Ala63=
ENST00000375263.7:c.188C=	ENSP00000364412.3:p.Ala63=
NM_000197.1:c.188C=	NP_000188.1:p.Ala63=
XM_006717095.2:c.188C=	XP_006717158.1:p.Ala63=
XM_011518618.1:c.188C=	XP_011516920.1:p.Ala63=
XM_011518619.1:c.188C=	XP_011516921.1:p.Ala63=
XM_011518620.1:c.188C=	XP_011516922.1:p.Ala63=
XM_011518621.1:c.188C=	XP_011516923.1:p.Ala63=
NM_000197.2:c.188C= MANE Select	NP_000188.1:p.Ala63=
XM_011518618.2:c.188C=	XP_011516920.1:p.Ala63=
XM_011518619.2:c.188C=	XP_011516921.1:p.Ala63=
XM_017014671.1:c.188C=	XP_016870160.1:p.Ala63=
XM_017014672.1:c.188C=	XP_016870161.1:p.Ala63=
XM_017014673.2:c.188C=	XP_016870162.1:p.Ala63=
XM_017014674.1:c.188C=	XP_016870163.1:p.Ala63=
XM_017014675.1:c.102C=	XP_016870164.1:p.Ser34=
XM_017014677.1:c.-749C=	XP_016870166.1:n.-749C=
XM_024447529.1:c.102C=	XP_024303297.1:p.Ser34=
XR_002956778.1:n.2622C=