Canonical Allele Identifier: CA466129716

Gene: HSD17B3

Linked Data

• MyVariant Identifiers: chr9:g.98997837G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96235555G>A , CM000671.2:g.96235555G>A	GRCh38
NC_000009.11:g.98997837G>A , CM000671.1:g.98997837G>A	GRCh37
NC_000009.10:g.98037658G>A	NCBI36
NG_008157.1:g.71598C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.688C>T	ENSP00000364411.2:p.Leu230=
ENST00000375263.8:c.838C>T MANE Select	ENSP00000364412.3:p.Leu280=
ENST00000463517.2:n.2380C>T
ENST00000464104.6:n.1776C>T
ENST00000467499.6:c.*537C>T	ENSP00000498077.1:n.*537C>T
ENST00000494814.6:n.388C>T
ENST00000643789.1:c.3130C>T
ENST00000648146.1:c.976C>T	ENSP00000497238.1:n.976C>T
ENST00000648332.1:c.515C>T	ENSP00000497562.1:n.515C>T
ENST00000648799.1:c.730C>T	ENSP00000498039.1:p.Leu244=
ENST00000650005.1:c.767C>T	ENSP00000498121.1:n.767C>T
ENST00000375262.3:c.688C>T	ENSP00000364411.2:p.Leu230=
ENST00000375263.7:c.838C>T	ENSP00000364412.3:p.Leu280=
ENST00000464104.5:n.691C>T
ENST00000467499.5:n.98C>T
ENST00000494814.5:n.397C>T
NM_000197.1:c.838C>T	NP_000188.1:p.Leu280=
XM_005251970.3:c.478C>T	XP_005252027.1:p.Leu160=
XM_011518618.1:c.838C>T	XP_011516920.1:p.Leu280=
XM_011518619.1:c.838C>T	XP_011516921.1:p.Leu280=
XM_011518620.1:c.730C>T	XP_011516922.1:p.Leu244=
NM_000197.2:c.838C>T MANE Select	NP_000188.1:p.Leu280=
XM_011518618.2:c.838C>T	XP_011516920.1:p.Leu280=
XM_011518619.2:c.838C>T	XP_011516921.1:p.Leu280=
XM_017014671.1:c.838C>T	XP_016870160.1:p.Leu280=
XM_017014672.1:c.838C>T	XP_016870161.1:p.Leu280=
XM_017014673.2:c.802C>T	XP_016870162.1:p.Leu268=
XM_017014674.1:c.730C>T	XP_016870163.1:p.Leu244=
XM_017014675.1:c.676C>T	XP_016870164.1:p.Leu226=
XM_017014677.1:c.478C>T	XP_016870166.1:p.Leu160=
XM_024447529.1:c.676C>T	XP_024303297.1:p.Leu226=
XR_002956778.1:n.3310C>T