Canonical Allele Identifier: CA374121954

Gene: HSD17B3

Linked Data

• MyVariant Identifiers: chr9:g.98997827G>A (hg19) ; chr9:g.96235545G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96235545G>A , CM000671.2:g.96235545G>A	GRCh38
NC_000009.11:g.98997827G>A , CM000671.1:g.98997827G>A	GRCh37
NC_000009.10:g.98037648G>A	NCBI36
NG_008157.1:g.71608C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.698C>T	ENSP00000364411.2:p.Ala233Val
ENST00000375263.8:c.848C>T MANE Select	ENSP00000364412.3:p.Ala283Val
ENST00000463517.2:n.2390C>T
ENST00000464104.6:n.1786C>T
ENST00000467499.6:c.*547C>T	ENSP00000498077.1:n.*547C>T
ENST00000494814.6:n.398C>T
ENST00000643789.1:c.3140C>T
ENST00000648146.1:c.986C>T	ENSP00000497238.1:n.986C>T
ENST00000648332.1:c.525C>T	ENSP00000497562.1:n.525C>T
ENST00000650005.1:c.777C>T	ENSP00000498121.1:n.777C>T
ENST00000375262.3:c.698C>T	ENSP00000364411.2:p.Ala233Val
ENST00000375263.7:c.848C>T	ENSP00000364412.3:p.Ala283Val
ENST00000464104.5:n.701C>T
ENST00000467499.5:n.108C>T
ENST00000494814.5:n.407C>T
NM_000197.1:c.848C>T	NP_000188.1:p.Ala283Val
XM_005251970.3:c.488C>T	XP_005252027.1:p.Ala163Val
XM_011518618.1:c.848C>T	XP_011516920.1:p.Ala283Val
XM_011518619.1:c.848C>T	XP_011516921.1:p.Ala283Val
XM_011518620.1:c.740C>T	XP_011516922.1:p.Ala247Val
NM_000197.2:c.848C>T MANE Select	NP_000188.1:p.Ala283Val
XM_011518618.2:c.848C>T	XP_011516920.1:p.Ala283Val
XM_011518619.2:c.848C>T	XP_011516921.1:p.Ala283Val
XM_017014671.1:c.848C>T	XP_016870160.1:p.Ala283Val
XM_017014672.1:c.848C>T	XP_016870161.1:p.Ala283Val
XM_017014673.2:c.812C>T	XP_016870162.1:p.Ala271Val
XM_017014674.1:c.740C>T	XP_016870163.1:p.Ala247Val
XM_017014675.1:c.686C>T	XP_016870164.1:p.Ala229Val
XM_017014677.1:c.488C>T	XP_016870166.1:p.Ala163Val
XM_024447529.1:c.686C>T	XP_024303297.1:p.Ala229Val
XR_002956778.1:n.3320C>T