Canonical Allele Identifier: CA1865974686

Gene: HSD17B3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96235491G= , CM000671.2:g.96235491G=	GRCh38
NC_000009.11:g.98997773G= , CM000671.1:g.98997773G=	GRCh37
NC_000009.10:g.98037594G=	NCBI36
NG_008157.1:g.71662C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.752C=	ENSP00000364411.2:p.Ala251=
ENST00000375263.8:c.902C= MANE Select	ENSP00000364412.3:p.Ala301=
ENST00000463517.2:n.2444C=
ENST00000464104.6:n.1840C=
ENST00000467499.6:c.*601C=	ENSP00000498077.1:n.*601C=
ENST00000494814.6:n.452C=
ENST00000643789.1:c.3194C=
ENST00000648146.1:c.1040C=	ENSP00000497238.1:n.1040C=
ENST00000648332.1:c.579C=	ENSP00000497562.1:n.579C=
ENST00000650005.1:c.831C=	ENSP00000498121.1:n.831C=
ENST00000375262.3:c.752C=	ENSP00000364411.2:p.Ala251=
ENST00000375263.7:c.902C=	ENSP00000364412.3:p.Ala301=
ENST00000464104.5:n.755C=
ENST00000467499.5:n.162C=
ENST00000494814.5:n.461C=
NM_000197.1:c.902C=	NP_000188.1:p.Ala301=
XM_005251970.3:c.542C=	XP_005252027.1:p.Ala181=
XM_011518618.1:c.902C=	XP_011516920.1:p.Ala301=
XM_011518619.1:c.902C=	XP_011516921.1:p.Ala301=
XM_011518620.1:c.794C=	XP_011516922.1:p.Ala265=
NM_000197.2:c.902C= MANE Select	NP_000188.1:p.Ala301=
XM_011518618.2:c.902C=	XP_011516920.1:p.Ala301=
XM_011518619.2:c.902C=	XP_011516921.1:p.Ala301=
XM_017014671.1:c.902C=	XP_016870160.1:p.Ala301=
XM_017014672.1:c.902C=	XP_016870161.1:p.Ala301=
XM_017014673.2:c.866C=	XP_016870162.1:p.Ala289=
XM_017014674.1:c.794C=	XP_016870163.1:p.Ala265=
XM_017014675.1:c.740C=	XP_016870164.1:p.Ala247=
XM_017014677.1:c.542C=	XP_016870166.1:p.Ala181=
XM_024447529.1:c.740C=	XP_024303297.1:p.Ala247=
XR_002956778.1:n.3374C=