Canonical Allele Identifier: CA2785195905

Gene: HSD17B3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96240990_96240991insAACA , CM000671.2:g.96240990_96240991insAACA	GRCh38
NC_000009.11:g.99003272_99003273insAACA , CM000671.1:g.99003272_99003273insAACA	GRCh37
NC_000009.10:g.98043093_98043094insAACA	NCBI36
NG_008157.1:g.66162_66163insTGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.672+3338_672+3339insTGTT	ENSP00000364411.2:n.672+3338_672+3339insTGTT
ENST00000375263.8:c.673-84_673-83insTGTT MANE Select	ENSP00000364412.3:n.673-84_673-83insTGTT
ENST00000463517.2:n.2215-84_2215-83insTGTT
ENST00000464104.6:n.1611-84_1611-83insTGTT
ENST00000467499.6:c.*372-84_*372-83insTGTT	ENSP00000498077.1:n.*372-84_*372-83insTGTT
ENST00000484816.2:n.24-84_24-83insTGTT
ENST00000494814.6:n.223-84_223-83insTGTT
ENST00000643789.1:c.2965-84_2965-83insTGTT
ENST00000648146.1:c.673-84_673-83insTGTT	ENSP00000497238.1:n.673-84_673-83insTGTT
ENST00000648332.1:c.350-84_350-83insTGTT	ENSP00000497562.1:n.350-84_350-83insTGTT
ENST00000648799.1:c.565-84_565-83insTGTT	ENSP00000498039.1:n.565-84_565-83insTGTT
ENST00000650005.1:c.602-84_602-83insTGTT	ENSP00000498121.1:n.602-84_602-83insTGTT
ENST00000375262.3:c.672+3338_672+3339insTGTT	ENSP00000364411.2:n.672+3338_672+3339insTGTT
ENST00000375263.7:c.673-84_673-83insTGTT	ENSP00000364412.3:n.673-84_673-83insTGTT
ENST00000464104.5:n.526-84_526-83insTGTT
ENST00000484816.1:n.23-84_23-83insTGTT
ENST00000494814.5:n.232-84_232-83insTGTT
NM_000197.1:c.673-84_673-83insTGTT	NP_000188.1:n.673-84_673-83insTGTT
XM_005251970.3:c.313-84_313-83insTGTT	XP_005252027.1:n.313-84_313-83insTGTT
XM_011518618.1:c.673-84_673-83insTGTT	XP_011516920.1:n.673-84_673-83insTGTT
XM_011518619.1:c.673-84_673-83insTGTT	XP_011516921.1:n.673-84_673-83insTGTT
XM_011518620.1:c.565-84_565-83insTGTT	XP_011516922.1:n.565-84_565-83insTGTT
XM_011518621.1:c.711-84_711-83insTGTT	XP_011516923.1:n.711-84_711-83insTGTT
NM_000197.2:c.673-84_673-83insTGTT MANE Select	NP_000188.1:n.673-84_673-83insTGTT
XM_011518618.2:c.673-84_673-83insTGTT	XP_011516920.1:n.673-84_673-83insTGTT
XM_011518619.2:c.673-84_673-83insTGTT	XP_011516921.1:n.673-84_673-83insTGTT
XM_017014671.1:c.673-84_673-83insTGTT	XP_016870160.1:n.673-84_673-83insTGTT
XM_017014672.1:c.673-84_673-83insTGTT	XP_016870161.1:n.673-84_673-83insTGTT
XM_017014673.2:c.637-84_637-83insTGTT	XP_016870162.1:n.637-84_637-83insTGTT
XM_017014674.1:c.565-84_565-83insTGTT	XP_016870163.1:n.565-84_565-83insTGTT
XM_017014675.1:c.511-84_511-83insTGTT	XP_016870164.1:n.511-84_511-83insTGTT
XM_017014677.1:c.313-84_313-83insTGTT	XP_016870166.1:n.313-84_313-83insTGTT
XM_024447529.1:c.511-84_511-83insTGTT	XP_024303297.1:n.511-84_511-83insTGTT
XR_002956778.1:n.3145-84_3145-83insTGTT