Canonical Allele Identifier: CA1865987847

Gene: HSD17B3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96244386C= , CM000671.2:g.96244386C=	GRCh38
NC_000009.11:g.99006668C= , CM000671.1:g.99006668C=	GRCh37
NC_000009.10:g.98046489C=	NCBI36
NG_008157.1:g.62767G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.615G=	ENSP00000364411.2:p.Val205=
ENST00000375263.8:c.615G= MANE Select	ENSP00000364412.3:p.Val205=
ENST00000463517.2:n.2157G=
ENST00000464104.6:n.1553G=
ENST00000467499.6:c.*314G=	ENSP00000498077.1:n.*314G=
ENST00000494814.6:n.127G=
ENST00000643789.1:c.2907G=
ENST00000648146.1:c.615G=	ENSP00000497238.1:p.Val205=
ENST00000648332.1:c.292G=	ENSP00000497562.1:p.Val98=
ENST00000648799.1:c.507G=	ENSP00000498039.1:p.Val169=
ENST00000650005.1:c.544G=	ENSP00000498121.1:p.Val182=
ENST00000375262.3:c.615G=	ENSP00000364411.2:p.Val205=
ENST00000375263.7:c.615G=	ENSP00000364412.3:p.Val205=
ENST00000464104.5:n.468G=
ENST00000494814.5:n.136G=
NM_000197.1:c.615G=	NP_000188.1:p.Val205=
XM_005251970.3:c.255G=	XP_005252027.1:p.Val85=
XM_011518618.1:c.615G=	XP_011516920.1:p.Val205=
XM_011518619.1:c.615G=	XP_011516921.1:p.Val205=
XM_011518620.1:c.507G=	XP_011516922.1:p.Val169=
XM_011518621.1:c.615G=	XP_011516923.1:p.Val205=
NM_000197.2:c.615G= MANE Select	NP_000188.1:p.Val205=
XM_011518618.2:c.615G=	XP_011516920.1:p.Val205=
XM_011518619.2:c.615G=	XP_011516921.1:p.Val205=
XM_017014671.1:c.615G=	XP_016870160.1:p.Val205=
XM_017014672.1:c.615G=	XP_016870161.1:p.Val205=
XM_017014673.2:c.579G=	XP_016870162.1:p.Val193=
XM_017014674.1:c.507G=	XP_016870163.1:p.Val169=
XM_017014675.1:c.453G=	XP_016870164.1:p.Val151=
XM_017014677.1:c.255G=	XP_016870166.1:p.Val85=
XM_024447529.1:c.453G=	XP_024303297.1:p.Val151=
XR_002956778.1:n.3049G=