Canonical Allele Identifier: CA1577006821

Gene: HSD17B4

Linked Data

• dbSNP Id: rs1580480437

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.119452497A>C , CM000667.2:g.119452497A>C	GRCh38
NC_000005.9:g.118788192A>C , CM000667.1:g.118788192A>C	GRCh37
NC_000005.8:g.118816091A>C	NCBI36
NG_008182.1:g.5045A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509514.6:c.-79A>C	ENSP00000426272.2:n.-79A>C
ENST00000682996.1:c.-79A>C	ENSP00000507792.1:n.-79A>C
ENST00000683936.1:c.-79A>C	ENSP00000507721.1:n.-79A>C
ENST00000683974.1:n.4A>C
ENST00000684214.1:c.-79A>C	ENSP00000508071.1:n.-79A>C
ENST00000414835.7:c.-257A>C	ENSP00000411960.3:n.-257A>C
ENST00000510025.7:c.-79A>C MANE Select	ENSP00000424940.3:n.-79A>C
ENST00000646590.1:c.-79A>C	ENSP00000494892.1:n.-79A>C
ENST00000256216.10:c.-79A>C	ENSP00000256216.6:n.-79A>C
ENST00000442060.7:c.-79A>C	ENSP00000390208.3:n.-79A>C
ENST00000511186.5:n.25A>C
ENST00000515320.5:c.-79A>C	ENSP00000424613.1:n.-79A>C
NM_000414.3:c.-79A>C	NP_000405.1:n.-79A>C
NM_001199291.2:c.-257A>C	NP_001186220.1:n.-257A>C
NM_001199292.1:c.-79A>C	NP_001186221.1:n.-79A>C
NM_001292027.1:c.-216A>C	NP_001278956.1:n.-216A>C
NM_001292028.1:c.-678A>C	NP_001278957.1:n.-678A>C
NM_000414.4:c.-79A>C MANE Select	NP_000405.1:n.-79A>C
NM_001199291.3:c.-257A>C	NP_001186220.1:n.-257A>C
NM_001199292.2:c.-79A>C	NP_001186221.1:n.-79A>C
NM_001292027.2:c.-216A>C	NP_001278956.1:n.-216A>C
NM_001292028.2:c.-678A>C	NP_001278957.1:n.-678A>C
NM_001374497.1:c.-79A>C	NP_001361426.1:n.-79A>C
NM_001374498.1:c.-79A>C	NP_001361427.1:n.-79A>C
NM_001374499.1:c.-612A>C	NP_001361428.1:n.-612A>C
NM_001374500.1:c.-805A>C	NP_001361429.1:n.-805A>C
NM_001374501.1:c.-678A>C	NP_001361430.1:n.-678A>C
NM_001374502.1:c.-683A>C	NP_001361431.1:n.-683A>C
NM_001374503.1:c.-748A>C	NP_001361432.1:n.-748A>C
NR_164653.1:n.1A>C
NR_164654.1:n.1A>C