Canonical Allele Identifier: CA1577006854
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119452535G= , CM000667.2:g.119452535G= GRCh38
NC_000005.9:g.118788230G= , CM000667.1:g.118788230G= GRCh37
NC_000005.8:g.118816129G= NCBI36
NG_008182.1:g.5083G=

Transcript Alleles

HGVS Amino-acid change
ENST00000509514.6:c.-41G= ENSP00000426272.2:n.-41G=
ENST00000512841.6:n.1G=
ENST00000518349.6:c.-41G= ENSP00000507185.1:n.-41G=
ENST00000682445.1:c.-41G= ENSP00000508061.1:n.-41G=
ENST00000682996.1:c.-41G= ENSP00000507792.1:n.-41G=
ENST00000683371.1:c.-41G= ENSP00000508376.1:n.-41G=
ENST00000683390.1:n.8G=
ENST00000683936.1:c.-41G= ENSP00000507721.1:n.-41G=
ENST00000683974.1:n.42G=
ENST00000684214.1:c.-41G= ENSP00000508071.1:n.-41G=
ENST00000414835.7:c.-219G= ENSP00000411960.3:n.-219G=
ENST00000510025.7:c.-41G= MANE Select ENSP00000424940.3:n.-41G=
ENST00000646058.1:c.-41G= ENSP00000493579.1:n.-41G=
ENST00000646590.1:c.-41G= ENSP00000494892.1:n.-41G=
ENST00000256216.10:c.-41G= ENSP00000256216.6:n.-41G=
ENST00000442060.7:c.-41G= ENSP00000390208.3:n.-41G=
ENST00000511186.5:n.63G=
ENST00000515235.6:n.20G=
ENST00000515320.5:c.-41G= ENSP00000424613.1:n.-41G=
NM_000414.3:c.-41G= NP_000405.1:n.-41G=
NM_001199291.2:c.-219G= NP_001186220.1:n.-219G=
NM_001199292.1:c.-41G= NP_001186221.1:n.-41G=
NM_001292027.1:c.-178G= NP_001278956.1:n.-178G=
NM_001292028.1:c.-640G= NP_001278957.1:n.-640G=
NM_000414.4:c.-41G= MANE Select NP_000405.1:n.-41G=
NM_001199291.3:c.-219G= NP_001186220.1:n.-219G=
NM_001199292.2:c.-41G= NP_001186221.1:n.-41G=
NM_001292027.2:c.-178G= NP_001278956.1:n.-178G=
NM_001292028.2:c.-640G= NP_001278957.1:n.-640G=
NM_001374497.1:c.-41G= NP_001361426.1:n.-41G=
NM_001374498.1:c.-41G= NP_001361427.1:n.-41G=
NM_001374499.1:c.-574G= NP_001361428.1:n.-574G=
NM_001374500.1:c.-767G= NP_001361429.1:n.-767G=
NM_001374501.1:c.-640G= NP_001361430.1:n.-640G=
NM_001374502.1:c.-645G= NP_001361431.1:n.-645G=
NM_001374503.1:c.-710G= NP_001361432.1:n.-710G=
NR_164653.1:n.39G=
NR_164654.1:n.39G=