Canonical Allele Identifier: CA374121833

Gene: HSD17B3

Linked Data

• MyVariant Identifiers: chr9:g.98997802G>T (hg19) ; chr9:g.96235520G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96235520G>T , CM000671.2:g.96235520G>T	GRCh38
NC_000009.11:g.98997802G>T , CM000671.1:g.98997802G>T	GRCh37
NC_000009.10:g.98037623G>T	NCBI36
NG_008157.1:g.71633C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.723C>A	ENSP00000364411.2:p.Phe241Leu
ENST00000375263.8:c.873C>A MANE Select	ENSP00000364412.3:p.Phe291Leu
ENST00000463517.2:n.2415C>A
ENST00000464104.6:n.1811C>A
ENST00000467499.6:c.*572C>A	ENSP00000498077.1:n.*572C>A
ENST00000494814.6:n.423C>A
ENST00000643789.1:c.3165C>A
ENST00000648146.1:c.1011C>A	ENSP00000497238.1:n.1011C>A
ENST00000648332.1:c.550C>A	ENSP00000497562.1:n.550C>A
ENST00000650005.1:c.802C>A	ENSP00000498121.1:n.802C>A
ENST00000375262.3:c.723C>A	ENSP00000364411.2:p.Phe241Leu
ENST00000375263.7:c.873C>A	ENSP00000364412.3:p.Phe291Leu
ENST00000464104.5:n.726C>A
ENST00000467499.5:n.133C>A
ENST00000494814.5:n.432C>A
NM_000197.1:c.873C>A	NP_000188.1:p.Phe291Leu
XM_005251970.3:c.513C>A	XP_005252027.1:p.Phe171Leu
XM_011518618.1:c.873C>A	XP_011516920.1:p.Phe291Leu
XM_011518619.1:c.873C>A	XP_011516921.1:p.Phe291Leu
XM_011518620.1:c.765C>A	XP_011516922.1:p.Phe255Leu
NM_000197.2:c.873C>A MANE Select	NP_000188.1:p.Phe291Leu
XM_011518618.2:c.873C>A	XP_011516920.1:p.Phe291Leu
XM_011518619.2:c.873C>A	XP_011516921.1:p.Phe291Leu
XM_017014671.1:c.873C>A	XP_016870160.1:p.Phe291Leu
XM_017014672.1:c.873C>A	XP_016870161.1:p.Phe291Leu
XM_017014673.2:c.837C>A	XP_016870162.1:p.Phe279Leu
XM_017014674.1:c.765C>A	XP_016870163.1:p.Phe255Leu
XM_017014675.1:c.711C>A	XP_016870164.1:p.Phe237Leu
XM_017014677.1:c.513C>A	XP_016870166.1:p.Phe171Leu
XM_024447529.1:c.711C>A	XP_024303297.1:p.Phe237Leu
XR_002956778.1:n.3345C>A