Canonical Allele Identifier: CA2674977142

Gene: HSD17B4

Linked Data

• gnomAD v4: 5-119452507-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.119452507T>A , CM000667.2:g.119452507T>A	GRCh38
NC_000005.9:g.118788202T>A , CM000667.1:g.118788202T>A	GRCh37
NC_000005.8:g.118816101T>A	NCBI36
NG_008182.1:g.5055T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509514.6:c.-69T>A	ENSP00000426272.2:n.-69T>A
ENST00000682996.1:c.-69T>A	ENSP00000507792.1:n.-69T>A
ENST00000683936.1:c.-69T>A	ENSP00000507721.1:n.-69T>A
ENST00000683974.1:n.14T>A
ENST00000684214.1:c.-69T>A	ENSP00000508071.1:n.-69T>A
ENST00000414835.7:c.-247T>A	ENSP00000411960.3:n.-247T>A
ENST00000510025.7:c.-69T>A MANE Select	ENSP00000424940.3:n.-69T>A
ENST00000646590.1:c.-69T>A	ENSP00000494892.1:n.-69T>A
ENST00000256216.10:c.-69T>A	ENSP00000256216.6:n.-69T>A
ENST00000442060.7:c.-69T>A	ENSP00000390208.3:n.-69T>A
ENST00000511186.5:n.35T>A
ENST00000515320.5:c.-69T>A	ENSP00000424613.1:n.-69T>A
NM_000414.3:c.-69T>A	NP_000405.1:n.-69T>A
NM_001199291.2:c.-247T>A	NP_001186220.1:n.-247T>A
NM_001199292.1:c.-69T>A	NP_001186221.1:n.-69T>A
NM_001292027.1:c.-206T>A	NP_001278956.1:n.-206T>A
NM_001292028.1:c.-668T>A	NP_001278957.1:n.-668T>A
NM_000414.4:c.-69T>A MANE Select	NP_000405.1:n.-69T>A
NM_001199291.3:c.-247T>A	NP_001186220.1:n.-247T>A
NM_001199292.2:c.-69T>A	NP_001186221.1:n.-69T>A
NM_001292027.2:c.-206T>A	NP_001278956.1:n.-206T>A
NM_001292028.2:c.-668T>A	NP_001278957.1:n.-668T>A
NM_001374497.1:c.-69T>A	NP_001361426.1:n.-69T>A
NM_001374498.1:c.-69T>A	NP_001361427.1:n.-69T>A
NM_001374499.1:c.-602T>A	NP_001361428.1:n.-602T>A
NM_001374500.1:c.-795T>A	NP_001361429.1:n.-795T>A
NM_001374501.1:c.-668T>A	NP_001361430.1:n.-668T>A
NM_001374502.1:c.-673T>A	NP_001361431.1:n.-673T>A
NM_001374503.1:c.-738T>A	NP_001361432.1:n.-738T>A
NR_164653.1:n.11T>A
NR_164654.1:n.11T>A