Canonical Allele Identifier: CA1865982967

Gene: HSD17B3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96240777C= , CM000671.2:g.96240777C=	GRCh38
NC_000009.11:g.99003059C= , CM000671.1:g.99003059C=	GRCh37
NC_000009.10:g.98042880C=	NCBI36
NG_008157.1:g.66376G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000197.2:c.803G= MANE Select	NP_000188.1:p.Cys268=
ENST00000375263.8:c.803G= MANE Select	ENSP00000364412.3:p.Cys268=
NM_000197.1:c.803G=	NP_000188.1:p.Cys268=
ENST00000375262.3:c.672+3552G=	ENSP00000364411.2:n.672+3552G=
ENST00000375262.4:c.672+3552G=	ENSP00000364411.2:n.672+3552G=
ENST00000375263.7:c.803G=	ENSP00000364412.3:p.Cys268=
ENST00000463517.2:n.2345G=
ENST00000464104.5:n.656G=
ENST00000464104.6:n.1741G=
ENST00000467499.6:c.*502G=	ENSP00000498077.1:n.*502G=
ENST00000484816.1:n.153G=
ENST00000484816.2:n.154G=
ENST00000494814.5:n.362G=
ENST00000494814.6:n.353G=
ENST00000643789.1:c.3095G=
ENST00000648146.1:c.803G=	ENSP00000497238.1:p.Cys268=
ENST00000648332.1:c.480G=	ENSP00000497562.1:n.480G=
ENST00000648799.1:c.695G=	ENSP00000498039.1:p.Cys232=
ENST00000650005.1:c.732G=	ENSP00000498121.1:n.732G=
XM_005251970.3:c.443G=	XP_005252027.1:p.Cys148=
XM_011518618.1:c.803G=	XP_011516920.1:p.Cys268=
XM_011518618.2:c.803G=	XP_011516920.1:p.Cys268=
XM_011518619.1:c.803G=	XP_011516921.1:p.Cys268=
XM_011518619.2:c.803G=	XP_011516921.1:p.Cys268=
XM_011518620.1:c.695G=	XP_011516922.1:p.Cys232=
XM_017014671.1:c.803G=	XP_016870160.1:p.Cys268=
XM_017014672.1:c.803G=	XP_016870161.1:p.Cys268=
XM_017014673.2:c.767G=	XP_016870162.1:p.Cys256=
XM_017014674.1:c.695G=	XP_016870163.1:p.Cys232=
XM_017014675.1:c.641G=	XP_016870164.1:p.Cys214=
XM_017014677.1:c.443G=	XP_016870166.1:p.Cys148=
XM_024447529.1:c.641G=	XP_024303297.1:p.Cys214=
XR_002956778.1:n.3275G=