Canonical Allele Identifier: CA1865987552

Gene: HSD17B3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96244157_96244173delinsAAAAGCCCACGTGGCAT , CM000671.2:g.96244157_96244173delinsAAAAGCCCACGTGGCAT	GRCh38
NC_000009.11:g.99006439_99006455delinsAAAAGCCCACGTGGCAT , CM000671.1:g.99006439_99006455delinsAAAAGCCCACGTGGCAT	GRCh37
NC_000009.10:g.98046260_98046276delinsAAAAGCCCACGTGGCAT	NCBI36
NG_008157.1:g.62980_62996delinsATGCCACGTGGGCTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.672+156_672+172delinsATGCCACGTGGGCTTTT	ENSP00000364411.2:n.672+156_672+172delinsATGCCACGTGGGCTTTT
ENST00000375263.8:c.672+156_672+172delinsATGCCACGTGGGCTTTT MANE Select	ENSP00000364412.3:n.672+156_672+172delinsATGCCACGTGGGCTTTT
ENST00000463517.2:n.2214+156_2214+172delinsATGCCACGTGGGCTTTT
ENST00000464104.6:n.1610+156_1610+172delinsATGCCACGTGGGCTTTT
ENST00000467499.6:c.*371+156_*371+172delinsATGCCACGTGGGCTTTT	ENSP00000498077.1:n.*371+156_*371+172delinsATGCCACGTGGGCTTTT
ENST00000484816.2:n.23+156_23+172delinsATGCCACGTGGGCTTTT
ENST00000494814.6:n.222+118_222+134delinsATGCCACGTGGGCTTTT
ENST00000643789.1:c.2964+156_2964+172delinsATGCCACGTGGGCTTTT
ENST00000648146.1:c.672+156_672+172delinsATGCCACGTGGGCTTTT	ENSP00000497238.1:n.672+156_672+172delinsATGCCACGTGGGCTTTT
ENST00000648332.1:c.349+156_349+172delinsATGCCACGTGGGCTTTT	ENSP00000497562.1:n.349+156_349+172delinsATGCCACGTGGGCTTTT
ENST00000648799.1:c.564+156_564+172delinsATGCCACGTGGGCTTTT	ENSP00000498039.1:n.564+156_564+172delinsATGCCACGTGGGCTTTT
ENST00000650005.1:c.601+156_601+172delinsATGCCACGTGGGCTTTT	ENSP00000498121.1:n.601+156_601+172delinsATGCCACGTGGGCTTTT
ENST00000375262.3:c.672+156_672+172delinsATGCCACGTGGGCTTTT	ENSP00000364411.2:n.672+156_672+172delinsATGCCACGTGGGCTTTT
ENST00000375263.7:c.672+156_672+172delinsATGCCACGTGGGCTTTT	ENSP00000364412.3:n.672+156_672+172delinsATGCCACGTGGGCTTTT
ENST00000464104.5:n.525+156_525+172delinsATGCCACGTGGGCTTTT
ENST00000484816.1:n.22+156_22+172delinsATGCCACGTGGGCTTTT
ENST00000494814.5:n.231+118_231+134delinsATGCCACGTGGGCTTTT
NM_000197.1:c.672+156_672+172delinsATGCCACGTGGGCTTTT	NP_000188.1:n.672+156_672+172delinsATGCCACGTGGGCTTTT
XM_005251970.3:c.312+156_312+172delinsATGCCACGTGGGCTTTT	XP_005252027.1:n.312+156_312+172delinsATGCCACGTGGGCTTTT
XM_011518618.1:c.672+156_672+172delinsATGCCACGTGGGCTTTT	XP_011516920.1:n.672+156_672+172delinsATGCCACGTGGGCTTTT
XM_011518619.1:c.672+156_672+172delinsATGCCACGTGGGCTTTT	XP_011516921.1:n.672+156_672+172delinsATGCCACGTGGGCTTTT
XM_011518620.1:c.564+156_564+172delinsATGCCACGTGGGCTTTT	XP_011516922.1:n.564+156_564+172delinsATGCCACGTGGGCTTTT
XM_011518621.1:c.710+118_710+134delinsATGCCACGTGGGCTTTT	XP_011516923.1:n.710+118_710+134delinsATGCCACGTGGGCTTTT
NM_000197.2:c.672+156_672+172delinsATGCCACGTGGGCTTTT MANE Select	NP_000188.1:n.672+156_672+172delinsATGCCACGTGGGCTTTT
XM_011518618.2:c.672+156_672+172delinsATGCCACGTGGGCTTTT	XP_011516920.1:n.672+156_672+172delinsATGCCACGTGGGCTTTT
XM_011518619.2:c.672+156_672+172delinsATGCCACGTGGGCTTTT	XP_011516921.1:n.672+156_672+172delinsATGCCACGTGGGCTTTT
XM_017014671.1:c.672+156_672+172delinsATGCCACGTGGGCTTTT	XP_016870160.1:n.672+156_672+172delinsATGCCACGTGGGCTTTT
XM_017014672.1:c.672+156_672+172delinsATGCCACGTGGGCTTTT	XP_016870161.1:n.672+156_672+172delinsATGCCACGTGGGCTTTT
XM_017014673.2:c.636+156_636+172delinsATGCCACGTGGGCTTTT	XP_016870162.1:n.636+156_636+172delinsATGCCACGTGGGCTTTT
XM_017014674.1:c.564+156_564+172delinsATGCCACGTGGGCTTTT	XP_016870163.1:n.564+156_564+172delinsATGCCACGTGGGCTTTT
XM_017014675.1:c.510+156_510+172delinsATGCCACGTGGGCTTTT	XP_016870164.1:n.510+156_510+172delinsATGCCACGTGGGCTTTT
XM_017014677.1:c.312+156_312+172delinsATGCCACGTGGGCTTTT	XP_016870166.1:n.312+156_312+172delinsATGCCACGTGGGCTTTT
XM_024447529.1:c.510+156_510+172delinsATGCCACGTGGGCTTTT	XP_024303297.1:n.510+156_510+172delinsATGCCACGTGGGCTTTT
XR_002956778.1:n.3144+118_3144+134delinsATGCCACGTGGGCTTTT