Canonical Allele Identifier: CA1865974332

Gene: HSD17B3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96235312G= , CM000671.2:g.96235312G=	GRCh38
NC_000009.11:g.98997594G= , CM000671.1:g.98997594G=	GRCh37
NC_000009.10:g.98037415G=	NCBI36
NG_008157.1:g.71841C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375263.8:c.*148C= MANE Select	ENSP00000364412.3:n.*148C=
ENST00000467499.6:c.*780C=	ENSP00000498077.1:n.*780C=
ENST00000494814.6:n.631C=
ENST00000375262.3:c.*148C=	ENSP00000364411.2:n.*148C=
ENST00000375263.7:c.*148C=	ENSP00000364412.3:n.*148C=
ENST00000464104.5:n.934C=
ENST00000467499.5:n.341C=
ENST00000494814.5:n.640C=
NM_000197.1:c.*148C=	NP_000188.1:n.*148C=
XM_005251970.3:c.*148C=	XP_005252027.1:n.*148C=
XM_011518618.1:c.*148C=	XP_011516920.1:n.*148C=
XM_011518619.1:c.*148C=	XP_011516921.1:n.*148C=
XM_011518620.1:c.*148C=	XP_011516922.1:n.*148C=
NM_000197.2:c.*148C= MANE Select	NP_000188.1:n.*148C=
XM_011518618.2:c.*148C=	XP_011516920.1:n.*148C=
XM_011518619.2:c.*148C=	XP_011516921.1:n.*148C=
XM_017014671.1:c.*148C=	XP_016870160.1:n.*148C=
XM_017014672.1:c.*148C=	XP_016870161.1:n.*148C=
XM_017014673.2:c.*148C=	XP_016870162.1:n.*148C=
XM_017014674.1:c.*148C=	XP_016870163.1:n.*148C=
XM_017014675.1:c.*148C=	XP_016870164.1:n.*148C=
XM_017014677.1:c.*148C=	XP_016870166.1:n.*148C=
XM_024447529.1:c.*148C=	XP_024303297.1:n.*148C=
XR_002956778.1:n.3553C=