Canonical Allele Identifier: CA374123336

Gene: HSD17B3

Linked Data

• MyVariant Identifiers: chr9:g.99003161G>T (hg19) ; chr9:g.96240879G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96240879G>T , CM000671.2:g.96240879G>T	GRCh38
NC_000009.11:g.99003161G>T , CM000671.1:g.99003161G>T	GRCh37
NC_000009.10:g.98042982G>T	NCBI36
NG_008157.1:g.66274C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000375262.4:c.672+3450C>A	ENSP00000364411.2:n.672+3450C>A
ENST00000375263.8:c.701C>A MANE Select	ENSP00000364412.3:p.Ala234Glu
ENST00000463517.2:n.2243C>A
ENST00000464104.6:n.1639C>A
ENST00000467499.6:c.*400C>A	ENSP00000498077.1:n.*400C>A
ENST00000484816.2:n.52C>A
ENST00000494814.6:n.251C>A
ENST00000643789.1:c.2993C>A
ENST00000648146.1:c.701C>A	ENSP00000497238.1:p.Ala234Glu
ENST00000648332.1:c.378C>A	ENSP00000497562.1:n.378C>A
ENST00000648799.1:c.593C>A	ENSP00000498039.1:p.Ala198Glu
ENST00000650005.1:c.630C>A	ENSP00000498121.1:n.630C>A
ENST00000375262.3:c.672+3450C>A	ENSP00000364411.2:n.672+3450C>A
ENST00000375263.7:c.701C>A	ENSP00000364412.3:p.Ala234Glu
ENST00000464104.5:n.554C>A
ENST00000484816.1:n.51C>A
ENST00000494814.5:n.260C>A
NM_000197.1:c.701C>A	NP_000188.1:p.Ala234Glu
XM_005251970.3:c.341C>A	XP_005252027.1:p.Ala114Glu
XM_011518618.1:c.701C>A	XP_011516920.1:p.Ala234Glu
XM_011518619.1:c.701C>A	XP_011516921.1:p.Ala234Glu
XM_011518620.1:c.593C>A	XP_011516922.1:p.Ala198Glu
XM_011518621.1:c.*22C>A	XP_011516923.1:n.*22C>A
NM_000197.2:c.701C>A MANE Select	NP_000188.1:p.Ala234Glu
XM_011518618.2:c.701C>A	XP_011516920.1:p.Ala234Glu
XM_011518619.2:c.701C>A	XP_011516921.1:p.Ala234Glu
XM_017014671.1:c.701C>A	XP_016870160.1:p.Ala234Glu
XM_017014672.1:c.701C>A	XP_016870161.1:p.Ala234Glu
XM_017014673.2:c.665C>A	XP_016870162.1:p.Ala222Glu
XM_017014674.1:c.593C>A	XP_016870163.1:p.Ala198Glu
XM_017014675.1:c.539C>A	XP_016870164.1:p.Ala180Glu
XM_017014677.1:c.341C>A	XP_016870166.1:p.Ala114Glu
XM_024447529.1:c.539C>A	XP_024303297.1:p.Ala180Glu
XR_002956778.1:n.3173C>A