Canonical Allele Identifier: CA1865974691

Gene: HSD17B3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96235495C= , CM000671.2:g.96235495C=	GRCh38
NC_000009.11:g.98997777C= , CM000671.1:g.98997777C=	GRCh37
NC_000009.10:g.98037598C=	NCBI36
NG_008157.1:g.71658G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.748G=	ENSP00000364411.2:p.Val250=
ENST00000375263.8:c.898G= MANE Select	ENSP00000364412.3:p.Val300=
ENST00000463517.2:n.2440G=
ENST00000464104.6:n.1836G=
ENST00000467499.6:c.*597G=	ENSP00000498077.1:n.*597G=
ENST00000494814.6:n.448G=
ENST00000643789.1:c.3190G=
ENST00000648146.1:c.1036G=	ENSP00000497238.1:n.1036G=
ENST00000648332.1:c.575G=	ENSP00000497562.1:n.575G=
ENST00000650005.1:c.827G=	ENSP00000498121.1:n.827G=
ENST00000375262.3:c.748G=	ENSP00000364411.2:p.Val250=
ENST00000375263.7:c.898G=	ENSP00000364412.3:p.Val300=
ENST00000464104.5:n.751G=
ENST00000467499.5:n.158G=
ENST00000494814.5:n.457G=
NM_000197.1:c.898G=	NP_000188.1:p.Val300=
XM_005251970.3:c.538G=	XP_005252027.1:p.Val180=
XM_011518618.1:c.898G=	XP_011516920.1:p.Val300=
XM_011518619.1:c.898G=	XP_011516921.1:p.Val300=
XM_011518620.1:c.790G=	XP_011516922.1:p.Val264=
NM_000197.2:c.898G= MANE Select	NP_000188.1:p.Val300=
XM_011518618.2:c.898G=	XP_011516920.1:p.Val300=
XM_011518619.2:c.898G=	XP_011516921.1:p.Val300=
XM_017014671.1:c.898G=	XP_016870160.1:p.Val300=
XM_017014672.1:c.898G=	XP_016870161.1:p.Val300=
XM_017014673.2:c.862G=	XP_016870162.1:p.Val288=
XM_017014674.1:c.790G=	XP_016870163.1:p.Val264=
XM_017014675.1:c.736G=	XP_016870164.1:p.Val246=
XM_017014677.1:c.538G=	XP_016870166.1:p.Val180=
XM_024447529.1:c.736G=	XP_024303297.1:p.Val246=
XR_002956778.1:n.3370G=