Canonical Allele Identifier: CA2785195756

Gene: HSD17B3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96235453C>A , CM000671.2:g.96235453C>A	GRCh38
NC_000009.11:g.98997735C>A , CM000671.1:g.98997735C>A	GRCh37
NC_000009.10:g.98037556C>A	NCBI36
NG_008157.1:g.71700G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000375263.8:c.*7G>T MANE Select	ENSP00000364412.3:n.*7G>T
ENST00000463517.2:n.2482G>T
ENST00000464104.6:n.1878G>T
ENST00000467499.6:c.*639G>T	ENSP00000498077.1:n.*639G>T
ENST00000494814.6:n.490G>T
ENST00000643789.1:c.3232G>T
ENST00000375262.3:c.*7G>T	ENSP00000364411.2:n.*7G>T
ENST00000375263.7:c.*7G>T	ENSP00000364412.3:n.*7G>T
ENST00000464104.5:n.793G>T
ENST00000467499.5:n.200G>T
ENST00000494814.5:n.499G>T
NM_000197.1:c.*7G>T	NP_000188.1:n.*7G>T
XM_005251970.3:c.*7G>T	XP_005252027.1:n.*7G>T
XM_011518618.1:c.*7G>T	XP_011516920.1:n.*7G>T
XM_011518619.1:c.*7G>T	XP_011516921.1:n.*7G>T
XM_011518620.1:c.*7G>T	XP_011516922.1:n.*7G>T
NM_000197.2:c.*7G>T MANE Select	NP_000188.1:n.*7G>T
XM_011518618.2:c.*7G>T	XP_011516920.1:n.*7G>T
XM_011518619.2:c.*7G>T	XP_011516921.1:n.*7G>T
XM_017014671.1:c.*7G>T	XP_016870160.1:n.*7G>T
XM_017014672.1:c.*7G>T	XP_016870161.1:n.*7G>T
XM_017014673.2:c.*7G>T	XP_016870162.1:n.*7G>T
XM_017014674.1:c.*7G>T	XP_016870163.1:n.*7G>T
XM_017014675.1:c.*7G>T	XP_016870164.1:n.*7G>T
XM_017014677.1:c.*7G>T	XP_016870166.1:n.*7G>T
XM_024447529.1:c.*7G>T	XP_024303297.1:n.*7G>T
XR_002956778.1:n.3412G>T