Canonical Allele Identifier: CA1865974641

Gene: HSD17B3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96235468C= , CM000671.2:g.96235468C=	GRCh38
NC_000009.11:g.98997750C= , CM000671.1:g.98997750C=	GRCh37
NC_000009.10:g.98037571C=	NCBI36
NG_008157.1:g.71685G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.775G=	ENSP00000364411.2:p.Val259=
ENST00000375263.8:c.925G= MANE Select	ENSP00000364412.3:p.Val309=
ENST00000463517.2:n.2467G=
ENST00000464104.6:n.1863G=
ENST00000467499.6:c.*624G=	ENSP00000498077.1:n.*624G=
ENST00000494814.6:n.475G=
ENST00000643789.1:c.3217G=
ENST00000648146.1:c.1063G=	ENSP00000497238.1:n.1063G=
ENST00000648332.1:c.602G=	ENSP00000497562.1:n.602G=
ENST00000650005.1:c.854G=	ENSP00000498121.1:n.854G=
ENST00000375262.3:c.775G=	ENSP00000364411.2:p.Val259=
ENST00000375263.7:c.925G=	ENSP00000364412.3:p.Val309=
ENST00000464104.5:n.778G=
ENST00000467499.5:n.185G=
ENST00000494814.5:n.484G=
NM_000197.1:c.925G=	NP_000188.1:p.Val309=
XM_005251970.3:c.565G=	XP_005252027.1:p.Val189=
XM_011518618.1:c.925G=	XP_011516920.1:p.Val309=
XM_011518619.1:c.925G=	XP_011516921.1:p.Val309=
XM_011518620.1:c.817G=	XP_011516922.1:p.Val273=
NM_000197.2:c.925G= MANE Select	NP_000188.1:p.Val309=
XM_011518618.2:c.925G=	XP_011516920.1:p.Val309=
XM_011518619.2:c.925G=	XP_011516921.1:p.Val309=
XM_017014671.1:c.925G=	XP_016870160.1:p.Val309=
XM_017014672.1:c.925G=	XP_016870161.1:p.Val309=
XM_017014673.2:c.889G=	XP_016870162.1:p.Val297=
XM_017014674.1:c.817G=	XP_016870163.1:p.Val273=
XM_017014675.1:c.763G=	XP_016870164.1:p.Val255=
XM_017014677.1:c.565G=	XP_016870166.1:p.Val189=
XM_024447529.1:c.763G=	XP_024303297.1:p.Val255=
XR_002956778.1:n.3397G=