Canonical Allele Identifier: CA374122046

Gene: HSD17B3

Linked Data

• MyVariant Identifiers: chr9:g.98997845A>G (hg19) ; chr9:g.96235563A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96235563A>G , CM000671.2:g.96235563A>G	GRCh38
NC_000009.11:g.98997845A>G , CM000671.1:g.98997845A>G	GRCh37
NC_000009.10:g.98037666A>G	NCBI36
NG_008157.1:g.71590T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.680T>C	ENSP00000364411.2:p.Phe227Ser
ENST00000375263.8:c.830T>C MANE Select	ENSP00000364412.3:p.Phe277Ser
ENST00000463517.2:n.2372T>C
ENST00000464104.6:n.1768T>C
ENST00000467499.6:c.*529T>C	ENSP00000498077.1:n.*529T>C
ENST00000494814.6:n.380T>C
ENST00000643789.1:c.3122T>C
ENST00000648146.1:c.968T>C	ENSP00000497238.1:n.968T>C
ENST00000648332.1:c.507T>C	ENSP00000497562.1:n.507T>C
ENST00000648799.1:c.722T>C	ENSP00000498039.1:p.Phe241Ser
ENST00000650005.1:c.759T>C	ENSP00000498121.1:n.759T>C
ENST00000375262.3:c.680T>C	ENSP00000364411.2:p.Phe227Ser
ENST00000375263.7:c.830T>C	ENSP00000364412.3:p.Phe277Ser
ENST00000464104.5:n.683T>C
ENST00000467499.5:n.90T>C
ENST00000494814.5:n.389T>C
NM_000197.1:c.830T>C	NP_000188.1:p.Phe277Ser
XM_005251970.3:c.470T>C	XP_005252027.1:p.Phe157Ser
XM_011518618.1:c.830T>C	XP_011516920.1:p.Phe277Ser
XM_011518619.1:c.830T>C	XP_011516921.1:p.Phe277Ser
XM_011518620.1:c.722T>C	XP_011516922.1:p.Phe241Ser
NM_000197.2:c.830T>C MANE Select	NP_000188.1:p.Phe277Ser
XM_011518618.2:c.830T>C	XP_011516920.1:p.Phe277Ser
XM_011518619.2:c.830T>C	XP_011516921.1:p.Phe277Ser
XM_017014671.1:c.830T>C	XP_016870160.1:p.Phe277Ser
XM_017014672.1:c.830T>C	XP_016870161.1:p.Phe277Ser
XM_017014673.2:c.794T>C	XP_016870162.1:p.Phe265Ser
XM_017014674.1:c.722T>C	XP_016870163.1:p.Phe241Ser
XM_017014675.1:c.668T>C	XP_016870164.1:p.Phe223Ser
XM_017014677.1:c.470T>C	XP_016870166.1:p.Phe157Ser
XM_024447529.1:c.668T>C	XP_024303297.1:p.Phe223Ser
XR_002956778.1:n.3302T>C