Canonical Allele Identifier: CA1865974885

Gene: HSD17B3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96235565G= , CM000671.2:g.96235565G=	GRCh38
NC_000009.11:g.98997847G= , CM000671.1:g.98997847G=	GRCh37
NC_000009.10:g.98037668G=	NCBI36
NG_008157.1:g.71588C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.678C=	ENSP00000364411.2:p.Gly226=
ENST00000375263.8:c.828C= MANE Select	ENSP00000364412.3:p.Gly276=
ENST00000463517.2:n.2370C=
ENST00000464104.6:n.1766C=
ENST00000467499.6:c.*527C=	ENSP00000498077.1:n.*527C=
ENST00000494814.6:n.378C=
ENST00000643789.1:c.3120C=
ENST00000648146.1:c.966C=	ENSP00000497238.1:n.966C=
ENST00000648332.1:c.505C=	ENSP00000497562.1:n.505C=
ENST00000648799.1:c.720C=	ENSP00000498039.1:p.Gly240=
ENST00000650005.1:c.757C=	ENSP00000498121.1:n.757C=
ENST00000375262.3:c.678C=	ENSP00000364411.2:p.Gly226=
ENST00000375263.7:c.828C=	ENSP00000364412.3:p.Gly276=
ENST00000464104.5:n.681C=
ENST00000467499.5:n.88C=
ENST00000494814.5:n.387C=
NM_000197.1:c.828C=	NP_000188.1:p.Gly276=
XM_005251970.3:c.468C=	XP_005252027.1:p.Gly156=
XM_011518618.1:c.828C=	XP_011516920.1:p.Gly276=
XM_011518619.1:c.828C=	XP_011516921.1:p.Gly276=
XM_011518620.1:c.720C=	XP_011516922.1:p.Gly240=
NM_000197.2:c.828C= MANE Select	NP_000188.1:p.Gly276=
XM_011518618.2:c.828C=	XP_011516920.1:p.Gly276=
XM_011518619.2:c.828C=	XP_011516921.1:p.Gly276=
XM_017014671.1:c.828C=	XP_016870160.1:p.Gly276=
XM_017014672.1:c.828C=	XP_016870161.1:p.Gly276=
XM_017014673.2:c.792C=	XP_016870162.1:p.Gly264=
XM_017014674.1:c.720C=	XP_016870163.1:p.Gly240=
XM_017014675.1:c.666C=	XP_016870164.1:p.Gly222=
XM_017014677.1:c.468C=	XP_016870166.1:p.Gly156=
XM_024447529.1:c.666C=	XP_024303297.1:p.Gly222=
XR_002956778.1:n.3300C=