Canonical Allele Identifier: CA1865974595

Gene: HSD17B3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96235457_96235458delinsTG , CM000671.2:g.96235457_96235458delinsTG	GRCh38
NC_000009.11:g.98997739_98997740delinsTG , CM000671.1:g.98997739_98997740delinsTG	GRCh37
NC_000009.10:g.98037560_98037561delinsTG	NCBI36
NG_008157.1:g.71695_71696delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000375263.8:c.*2_*3delinsCA MANE Select	ENSP00000364412.3:n.*2_*3delinsCA
ENST00000463517.2:n.2477_2478delinsCA
ENST00000464104.6:n.1873_1874delinsCA
ENST00000467499.6:c.*634_*635delinsCA	ENSP00000498077.1:n.*634_*635delinsCA
ENST00000494814.6:n.485_486delinsCA
ENST00000643789.1:c.3227_3228delinsCA
ENST00000375262.3:c.*2_*3delinsCA	ENSP00000364411.2:n.*2_*3delinsCA
ENST00000375263.7:c.*2_*3delinsCA	ENSP00000364412.3:n.*2_*3delinsCA
ENST00000464104.5:n.788_789delinsCA
ENST00000467499.5:n.195_196delinsCA
ENST00000494814.5:n.494_495delinsCA
NM_000197.1:c.*2_*3delinsCA	NP_000188.1:n.*2_*3delinsCA
XM_005251970.3:c.*2_*3delinsCA	XP_005252027.1:n.*2_*3delinsCA
XM_011518618.1:c.*2_*3delinsCA	XP_011516920.1:n.*2_*3delinsCA
XM_011518619.1:c.*2_*3delinsCA	XP_011516921.1:n.*2_*3delinsCA
XM_011518620.1:c.*2_*3delinsCA	XP_011516922.1:n.*2_*3delinsCA
NM_000197.2:c.*2_*3delinsCA MANE Select	NP_000188.1:n.*2_*3delinsCA
XM_011518618.2:c.*2_*3delinsCA	XP_011516920.1:n.*2_*3delinsCA
XM_011518619.2:c.*2_*3delinsCA	XP_011516921.1:n.*2_*3delinsCA
XM_017014671.1:c.*2_*3delinsCA	XP_016870160.1:n.*2_*3delinsCA
XM_017014672.1:c.*2_*3delinsCA	XP_016870161.1:n.*2_*3delinsCA
XM_017014673.2:c.*2_*3delinsCA	XP_016870162.1:n.*2_*3delinsCA
XM_017014674.1:c.*2_*3delinsCA	XP_016870163.1:n.*2_*3delinsCA
XM_017014675.1:c.*2_*3delinsCA	XP_016870164.1:n.*2_*3delinsCA
XM_017014677.1:c.*2_*3delinsCA	XP_016870166.1:n.*2_*3delinsCA
XM_024447529.1:c.*2_*3delinsCA	XP_024303297.1:n.*2_*3delinsCA
XR_002956778.1:n.3407_3408delinsCA