Canonical Allele Identifier: CA1865973784

Gene: HSD17B3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96298856_96298864delinsGCCCAGGCA , CM000671.2:g.96298856_96298864delinsGCCCAGGCA	GRCh38
NC_000009.11:g.99061138_99061146delinsGCCCAGGCA , CM000671.1:g.99061138_99061146delinsGCCCAGGCA	GRCh37
NC_000009.10:g.98100959_98100967delinsGCCCAGGCA	NCBI36
NG_008157.1:g.8289_8297delinsTGCCTGGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.155-402_155-394delinsTGCCTGGGC	ENSP00000364411.2:n.155-402_155-394delinsTGCCTGGGC
ENST00000375263.8:c.155-402_155-394delinsTGCCTGGGC MANE Select	ENSP00000364412.3:n.155-402_155-394delinsTGCCTGGGC
ENST00000463517.2:n.964-402_964-394delinsTGCCTGGGC
ENST00000464104.6:n.625-402_625-394delinsTGCCTGGGC
ENST00000467499.6:c.155-402_155-394delinsTGCCTGGGC	ENSP00000498077.1:n.155-402_155-394delinsTGCCTGGGC
ENST00000643789.1:c.2447-402_2447-394delinsTGCCTGGGC
ENST00000648146.1:c.155-402_155-394delinsTGCCTGGGC	ENSP00000497238.1:n.155-402_155-394delinsTGCCTGGGC
ENST00000648332.1:c.155-402_155-394delinsTGCCTGGGC	ENSP00000497562.1:n.155-402_155-394delinsTGCCTGGGC
ENST00000648799.1:c.155-402_155-394delinsTGCCTGGGC	ENSP00000498039.1:n.155-402_155-394delinsTGCCTGGGC
ENST00000650005.1:c.155-402_155-394delinsTGCCTGGGC	ENSP00000498121.1:n.155-402_155-394delinsTGCCTGGGC
ENST00000650386.1:c.155-402_155-394delinsTGCCTGGGC	ENSP00000497464.1:n.155-402_155-394delinsTGCCTGGGC
ENST00000375262.3:c.155-402_155-394delinsTGCCTGGGC	ENSP00000364411.2:n.155-402_155-394delinsTGCCTGGGC
ENST00000375263.7:c.155-402_155-394delinsTGCCTGGGC	ENSP00000364412.3:n.155-402_155-394delinsTGCCTGGGC
NM_000197.1:c.155-402_155-394delinsTGCCTGGGC	NP_000188.1:n.155-402_155-394delinsTGCCTGGGC
XM_006717095.2:c.155-402_155-394delinsTGCCTGGGC	XP_006717158.1:n.155-402_155-394delinsTGCCTGGGC
XM_011518618.1:c.155-402_155-394delinsTGCCTGGGC	XP_011516920.1:n.155-402_155-394delinsTGCCTGGGC
XM_011518619.1:c.155-402_155-394delinsTGCCTGGGC	XP_011516921.1:n.155-402_155-394delinsTGCCTGGGC
XM_011518620.1:c.155-402_155-394delinsTGCCTGGGC	XP_011516922.1:n.155-402_155-394delinsTGCCTGGGC
XM_011518621.1:c.155-402_155-394delinsTGCCTGGGC	XP_011516923.1:n.155-402_155-394delinsTGCCTGGGC
NM_000197.2:c.155-402_155-394delinsTGCCTGGGC MANE Select	NP_000188.1:n.155-402_155-394delinsTGCCTGGGC
XM_011518618.2:c.155-402_155-394delinsTGCCTGGGC	XP_011516920.1:n.155-402_155-394delinsTGCCTGGGC
XM_011518619.2:c.155-402_155-394delinsTGCCTGGGC	XP_011516921.1:n.155-402_155-394delinsTGCCTGGGC
XM_017014671.1:c.155-402_155-394delinsTGCCTGGGC	XP_016870160.1:n.155-402_155-394delinsTGCCTGGGC
XM_017014672.1:c.155-402_155-394delinsTGCCTGGGC	XP_016870161.1:n.155-402_155-394delinsTGCCTGGGC
XM_017014673.2:c.155-402_155-394delinsTGCCTGGGC	XP_016870162.1:n.155-402_155-394delinsTGCCTGGGC
XM_017014674.1:c.155-402_155-394delinsTGCCTGGGC	XP_016870163.1:n.155-402_155-394delinsTGCCTGGGC
XM_017014675.1:c.69-402_69-394delinsTGCCTGGGC	XP_016870164.1:n.69-402_69-394delinsTGCCTGGGC
XM_017014677.1:c.-782-402_-782-394delinsTGCCTGGGC	XP_016870166.1:n.-782-402_-782-394delinsTGCCTGGGC
XM_024447529.1:c.69-402_69-394delinsTGCCTGGGC	XP_024303297.1:n.69-402_69-394delinsTGCCTGGGC
XR_002956778.1:n.2589-402_2589-394delinsTGCCTGGGC