Canonical Allele Identifier: CA374123443

Gene: HSD17B3

Linked Data

• MyVariant Identifiers: chr9:g.99006621A>G (hg19) ; chr9:g.96244339A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96244339A>G , CM000671.2:g.96244339A>G	GRCh38
NC_000009.11:g.99006621A>G , CM000671.1:g.99006621A>G	GRCh37
NC_000009.10:g.98046442A>G	NCBI36
NG_008157.1:g.62814T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.662T>C	ENSP00000364411.2:p.Val221Ala
ENST00000375263.8:c.662T>C MANE Select	ENSP00000364412.3:p.Val221Ala
ENST00000463517.2:n.2204T>C
ENST00000464104.6:n.1600T>C
ENST00000467499.6:c.*361T>C	ENSP00000498077.1:n.*361T>C
ENST00000484816.2:n.13T>C
ENST00000494814.6:n.174T>C
ENST00000643789.1:c.2954T>C
ENST00000648146.1:c.662T>C	ENSP00000497238.1:p.Val221Ala
ENST00000648332.1:c.339T>C	ENSP00000497562.1:n.339T>C
ENST00000648799.1:c.554T>C	ENSP00000498039.1:p.Val185Ala
ENST00000650005.1:c.591T>C	ENSP00000498121.1:n.591T>C
ENST00000375262.3:c.662T>C	ENSP00000364411.2:p.Val221Ala
ENST00000375263.7:c.662T>C	ENSP00000364412.3:p.Val221Ala
ENST00000464104.5:n.515T>C
ENST00000484816.1:n.12T>C
ENST00000494814.5:n.183T>C
NM_000197.1:c.662T>C	NP_000188.1:p.Val221Ala
XM_005251970.3:c.302T>C	XP_005252027.1:p.Val101Ala
XM_011518618.1:c.662T>C	XP_011516920.1:p.Val221Ala
XM_011518619.1:c.662T>C	XP_011516921.1:p.Val221Ala
XM_011518620.1:c.554T>C	XP_011516922.1:p.Val185Ala
XM_011518621.1:c.662T>C	XP_011516923.1:p.Val221Ala
NM_000197.2:c.662T>C MANE Select	NP_000188.1:p.Val221Ala
XM_011518618.2:c.662T>C	XP_011516920.1:p.Val221Ala
XM_011518619.2:c.662T>C	XP_011516921.1:p.Val221Ala
XM_017014671.1:c.662T>C	XP_016870160.1:p.Val221Ala
XM_017014672.1:c.662T>C	XP_016870161.1:p.Val221Ala
XM_017014673.2:c.626T>C	XP_016870162.1:p.Val209Ala
XM_017014674.1:c.554T>C	XP_016870163.1:p.Val185Ala
XM_017014675.1:c.500T>C	XP_016870164.1:p.Val167Ala
XM_017014677.1:c.302T>C	XP_016870166.1:p.Val101Ala
XM_024447529.1:c.500T>C	XP_024303297.1:p.Val167Ala
XR_002956778.1:n.3096T>C