Canonical Allele Identifier: CA196616538

Gene: HSD17B3

Linked Data

• dbSNP Id: rs757506183
• gnomAD v2: 9-99006439-AAAAGCCCACGTGGCAT-A
• gnomAD v3: 9-96244157-AAAAGCCCACGTGGCAT-A
• gnomAD v4: 9-96244157-AAAAGCCCACGTGGCAT-A
• MyVariant Identifiers: chr9:g.99006440_99006455del (hg19) ; chr9:g.96244158_96244173del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96244158_96244173del , CM000671.2:g.96244158_96244173del	GRCh38
NC_000009.11:g.99006440_99006455del , CM000671.1:g.99006440_99006455del	GRCh37
NC_000009.10:g.98046261_98046276del	NCBI36
NG_008157.1:g.62980_62995del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.672+156_672+171del	ENSP00000364411.2:n.672+156_672+171del
ENST00000375263.8:c.672+156_672+171del MANE Select	ENSP00000364412.3:n.672+156_672+171del
ENST00000463517.2:n.2214+156_2214+171del
ENST00000464104.6:n.1610+156_1610+171del
ENST00000467499.6:c.*371+156_*371+171del	ENSP00000498077.1:n.*371+156_*371+171del
ENST00000484816.2:n.23+156_23+171del
ENST00000494814.6:n.222+118_222+133del
ENST00000643789.1:c.2964+156_2964+171del
ENST00000648146.1:c.672+156_672+171del	ENSP00000497238.1:n.672+156_672+171del
ENST00000648332.1:c.349+156_349+171del	ENSP00000497562.1:n.349+156_349+171del
ENST00000648799.1:c.564+156_564+171del	ENSP00000498039.1:n.564+156_564+171del
ENST00000650005.1:c.601+156_601+171del	ENSP00000498121.1:n.601+156_601+171del
ENST00000375262.3:c.672+156_672+171del	ENSP00000364411.2:n.672+156_672+171del
ENST00000375263.7:c.672+156_672+171del	ENSP00000364412.3:n.672+156_672+171del
ENST00000464104.5:n.525+156_525+171del
ENST00000484816.1:n.22+156_22+171del
ENST00000494814.5:n.231+118_231+133del
NM_000197.1:c.672+156_672+171del	NP_000188.1:n.672+156_672+171del
XM_005251970.3:c.312+156_312+171del	XP_005252027.1:n.312+156_312+171del
XM_011518618.1:c.672+156_672+171del	XP_011516920.1:n.672+156_672+171del
XM_011518619.1:c.672+156_672+171del	XP_011516921.1:n.672+156_672+171del
XM_011518620.1:c.564+156_564+171del	XP_011516922.1:n.564+156_564+171del
XM_011518621.1:c.710+118_710+133del	XP_011516923.1:n.710+118_710+133del
NM_000197.2:c.672+156_672+171del MANE Select	NP_000188.1:n.672+156_672+171del
XM_011518618.2:c.672+156_672+171del	XP_011516920.1:n.672+156_672+171del
XM_011518619.2:c.672+156_672+171del	XP_011516921.1:n.672+156_672+171del
XM_017014671.1:c.672+156_672+171del	XP_016870160.1:n.672+156_672+171del
XM_017014672.1:c.672+156_672+171del	XP_016870161.1:n.672+156_672+171del
XM_017014673.2:c.636+156_636+171del	XP_016870162.1:n.636+156_636+171del
XM_017014674.1:c.564+156_564+171del	XP_016870163.1:n.564+156_564+171del
XM_017014675.1:c.510+156_510+171del	XP_016870164.1:n.510+156_510+171del
XM_017014677.1:c.312+156_312+171del	XP_016870166.1:n.312+156_312+171del
XM_024447529.1:c.510+156_510+171del	XP_024303297.1:n.510+156_510+171del
XR_002956778.1:n.3144+118_3144+133del