Canonical Allele Identifier: CA1865974843

Gene: HSD17B3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96235547C= , CM000671.2:g.96235547C=	GRCh38
NC_000009.11:g.98997829C= , CM000671.1:g.98997829C=	GRCh37
NC_000009.10:g.98037650C=	NCBI36
NG_008157.1:g.71606G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.696G=	ENSP00000364411.2:p.Pro232=
ENST00000375263.8:c.846G= MANE Select	ENSP00000364412.3:p.Pro282=
ENST00000463517.2:n.2388G=
ENST00000464104.6:n.1784G=
ENST00000467499.6:c.*545G=	ENSP00000498077.1:n.*545G=
ENST00000494814.6:n.396G=
ENST00000643789.1:c.3138G=
ENST00000648146.1:c.984G=	ENSP00000497238.1:n.984G=
ENST00000648332.1:c.523G=	ENSP00000497562.1:n.523G=
ENST00000650005.1:c.775G=	ENSP00000498121.1:n.775G=
ENST00000375262.3:c.696G=	ENSP00000364411.2:p.Pro232=
ENST00000375263.7:c.846G=	ENSP00000364412.3:p.Pro282=
ENST00000464104.5:n.699G=
ENST00000467499.5:n.106G=
ENST00000494814.5:n.405G=
NM_000197.1:c.846G=	NP_000188.1:p.Pro282=
XM_005251970.3:c.486G=	XP_005252027.1:p.Pro162=
XM_011518618.1:c.846G=	XP_011516920.1:p.Pro282=
XM_011518619.1:c.846G=	XP_011516921.1:p.Pro282=
XM_011518620.1:c.738G=	XP_011516922.1:p.Pro246=
NM_000197.2:c.846G= MANE Select	NP_000188.1:p.Pro282=
XM_011518618.2:c.846G=	XP_011516920.1:p.Pro282=
XM_011518619.2:c.846G=	XP_011516921.1:p.Pro282=
XM_017014671.1:c.846G=	XP_016870160.1:p.Pro282=
XM_017014672.1:c.846G=	XP_016870161.1:p.Pro282=
XM_017014673.2:c.810G=	XP_016870162.1:p.Pro270=
XM_017014674.1:c.738G=	XP_016870163.1:p.Pro246=
XM_017014675.1:c.684G=	XP_016870164.1:p.Pro228=
XM_017014677.1:c.486G=	XP_016870166.1:p.Pro162=
XM_024447529.1:c.684G=	XP_024303297.1:p.Pro228=
XR_002956778.1:n.3318G=