Canonical Allele Identifier: CA1865974728

Gene: HSD17B3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96235514C= , CM000671.2:g.96235514C=	GRCh38
NC_000009.11:g.98997796C= , CM000671.1:g.98997796C=	GRCh37
NC_000009.10:g.98037617C=	NCBI36
NG_008157.1:g.71639G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.729G=	ENSP00000364411.2:p.Arg243=
ENST00000375263.8:c.879G= MANE Select	ENSP00000364412.3:p.Arg293=
ENST00000463517.2:n.2421G=
ENST00000464104.6:n.1817G=
ENST00000467499.6:c.*578G=	ENSP00000498077.1:n.*578G=
ENST00000494814.6:n.429G=
ENST00000643789.1:c.3171G=
ENST00000648146.1:c.1017G=	ENSP00000497238.1:n.1017G=
ENST00000648332.1:c.556G=	ENSP00000497562.1:n.556G=
ENST00000650005.1:c.808G=	ENSP00000498121.1:n.808G=
ENST00000375262.3:c.729G=	ENSP00000364411.2:p.Arg243=
ENST00000375263.7:c.879G=	ENSP00000364412.3:p.Arg293=
ENST00000464104.5:n.732G=
ENST00000467499.5:n.139G=
ENST00000494814.5:n.438G=
NM_000197.1:c.879G=	NP_000188.1:p.Arg293=
XM_005251970.3:c.519G=	XP_005252027.1:p.Arg173=
XM_011518618.1:c.879G=	XP_011516920.1:p.Arg293=
XM_011518619.1:c.879G=	XP_011516921.1:p.Arg293=
XM_011518620.1:c.771G=	XP_011516922.1:p.Arg257=
NM_000197.2:c.879G= MANE Select	NP_000188.1:p.Arg293=
XM_011518618.2:c.879G=	XP_011516920.1:p.Arg293=
XM_011518619.2:c.879G=	XP_011516921.1:p.Arg293=
XM_017014671.1:c.879G=	XP_016870160.1:p.Arg293=
XM_017014672.1:c.879G=	XP_016870161.1:p.Arg293=
XM_017014673.2:c.843G=	XP_016870162.1:p.Arg281=
XM_017014674.1:c.771G=	XP_016870163.1:p.Arg257=
XM_017014675.1:c.717G=	XP_016870164.1:p.Arg239=
XM_017014677.1:c.519G=	XP_016870166.1:p.Arg173=
XM_024447529.1:c.717G=	XP_024303297.1:p.Arg239=
XR_002956778.1:n.3351G=