Canonical Allele Identifier: CA374123612

Gene: HSD17B3

Linked Data

• MyVariant Identifiers: chr9:g.99006655T>G (hg19) ; chr9:g.96244373T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96244373T>G , CM000671.2:g.96244373T>G	GRCh38
NC_000009.11:g.99006655T>G , CM000671.1:g.99006655T>G	GRCh37
NC_000009.10:g.98046476T>G	NCBI36
NG_008157.1:g.62780A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.628A>C	ENSP00000364411.2:p.Lys210Gln
ENST00000375263.8:c.628A>C MANE Select	ENSP00000364412.3:p.Lys210Gln
ENST00000463517.2:n.2170A>C
ENST00000464104.6:n.1566A>C
ENST00000467499.6:c.*327A>C	ENSP00000498077.1:n.*327A>C
ENST00000494814.6:n.140A>C
ENST00000643789.1:c.2920A>C
ENST00000648146.1:c.628A>C	ENSP00000497238.1:p.Lys210Gln
ENST00000648332.1:c.305A>C	ENSP00000497562.1:p.Gln102Pro
ENST00000648799.1:c.520A>C	ENSP00000498039.1:p.Lys174Gln
ENST00000650005.1:c.557A>C	ENSP00000498121.1:p.Gln186Pro
ENST00000375262.3:c.628A>C	ENSP00000364411.2:p.Lys210Gln
ENST00000375263.7:c.628A>C	ENSP00000364412.3:p.Lys210Gln
ENST00000464104.5:n.481A>C
ENST00000494814.5:n.149A>C
NM_000197.1:c.628A>C	NP_000188.1:p.Lys210Gln
XM_005251970.3:c.268A>C	XP_005252027.1:p.Lys90Gln
XM_011518618.1:c.628A>C	XP_011516920.1:p.Lys210Gln
XM_011518619.1:c.628A>C	XP_011516921.1:p.Lys210Gln
XM_011518620.1:c.520A>C	XP_011516922.1:p.Lys174Gln
XM_011518621.1:c.628A>C	XP_011516923.1:p.Lys210Gln
NM_000197.2:c.628A>C MANE Select	NP_000188.1:p.Lys210Gln
XM_011518618.2:c.628A>C	XP_011516920.1:p.Lys210Gln
XM_011518619.2:c.628A>C	XP_011516921.1:p.Lys210Gln
XM_017014671.1:c.628A>C	XP_016870160.1:p.Lys210Gln
XM_017014672.1:c.628A>C	XP_016870161.1:p.Lys210Gln
XM_017014673.2:c.592A>C	XP_016870162.1:p.Lys198Gln
XM_017014674.1:c.520A>C	XP_016870163.1:p.Lys174Gln
XM_017014675.1:c.466A>C	XP_016870164.1:p.Lys156Gln
XM_017014677.1:c.268A>C	XP_016870166.1:p.Lys90Gln
XM_024447529.1:c.466A>C	XP_024303297.1:p.Lys156Gln
XR_002956778.1:n.3062A>C