Canonical Allele Identifier: CA374123592

Gene: HSD17B3

Linked Data

• MyVariant Identifiers: chr9:g.99006651G>T (hg19) ; chr9:g.96244369G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96244369G>T , CM000671.2:g.96244369G>T	GRCh38
NC_000009.11:g.99006651G>T , CM000671.1:g.99006651G>T	GRCh37
NC_000009.10:g.98046472G>T	NCBI36
NG_008157.1:g.62784C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.632C>A	ENSP00000364411.2:p.Ala211Asp
ENST00000375263.8:c.632C>A MANE Select	ENSP00000364412.3:p.Ala211Asp
ENST00000463517.2:n.2174C>A
ENST00000464104.6:n.1570C>A
ENST00000467499.6:c.*331C>A	ENSP00000498077.1:n.*331C>A
ENST00000494814.6:n.144C>A
ENST00000643789.1:c.2924C>A
ENST00000648146.1:c.632C>A	ENSP00000497238.1:p.Ala211Asp
ENST00000648332.1:c.309C>A	ENSP00000497562.1:p.Gly103=
ENST00000648799.1:c.524C>A	ENSP00000498039.1:p.Ala175Asp
ENST00000650005.1:c.561C>A	ENSP00000498121.1:p.Gly187=
ENST00000375262.3:c.632C>A	ENSP00000364411.2:p.Ala211Asp
ENST00000375263.7:c.632C>A	ENSP00000364412.3:p.Ala211Asp
ENST00000464104.5:n.485C>A
ENST00000494814.5:n.153C>A
NM_000197.1:c.632C>A	NP_000188.1:p.Ala211Asp
XM_005251970.3:c.272C>A	XP_005252027.1:p.Ala91Asp
XM_011518618.1:c.632C>A	XP_011516920.1:p.Ala211Asp
XM_011518619.1:c.632C>A	XP_011516921.1:p.Ala211Asp
XM_011518620.1:c.524C>A	XP_011516922.1:p.Ala175Asp
XM_011518621.1:c.632C>A	XP_011516923.1:p.Ala211Asp
NM_000197.2:c.632C>A MANE Select	NP_000188.1:p.Ala211Asp
XM_011518618.2:c.632C>A	XP_011516920.1:p.Ala211Asp
XM_011518619.2:c.632C>A	XP_011516921.1:p.Ala211Asp
XM_017014671.1:c.632C>A	XP_016870160.1:p.Ala211Asp
XM_017014672.1:c.632C>A	XP_016870161.1:p.Ala211Asp
XM_017014673.2:c.596C>A	XP_016870162.1:p.Ala199Asp
XM_017014674.1:c.524C>A	XP_016870163.1:p.Ala175Asp
XM_017014675.1:c.470C>A	XP_016870164.1:p.Ala157Asp
XM_017014677.1:c.272C>A	XP_016870166.1:p.Ala91Asp
XM_024447529.1:c.470C>A	XP_024303297.1:p.Ala157Asp
XR_002956778.1:n.3066C>A