Canonical Allele Identifier: CA2674977225

Gene: HSD17B4

Linked Data

• gnomAD v4: 5-119452733-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.119452733G>C , CM000667.2:g.119452733G>C	GRCh38
NC_000005.9:g.118788428G>C , CM000667.1:g.118788428G>C	GRCh37
NC_000005.8:g.118816327G>C	NCBI36
NG_008182.1:g.5281G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509514.6:c.58+100G>C	ENSP00000426272.2:n.58+100G>C
ENST00000512841.6:n.99+100G>C
ENST00000518349.6:c.58+100G>C	ENSP00000507185.1:n.58+100G>C
ENST00000682445.1:c.58+100G>C	ENSP00000508061.1:n.58+100G>C
ENST00000682531.1:n.6G>C
ENST00000682996.1:c.58+100G>C	ENSP00000507792.1:n.58+100G>C
ENST00000683371.1:c.58+100G>C	ENSP00000508376.1:n.58+100G>C
ENST00000683390.1:n.106+100G>C
ENST00000683936.1:c.58+100G>C	ENSP00000507721.1:n.58+100G>C
ENST00000683974.1:n.140+100G>C
ENST00000684214.1:c.58+100G>C	ENSP00000508071.1:n.58+100G>C
ENST00000414835.7:c.-21G>C	ENSP00000411960.3:n.-21G>C
ENST00000510025.7:c.58+100G>C MANE Select	ENSP00000424940.3:n.58+100G>C
ENST00000644146.1:c.58+100G>C	ENSP00000494808.1:n.58+100G>C
ENST00000645832.1:c.58+100G>C	ENSP00000494316.1:n.58+100G>C
ENST00000646058.1:c.58+100G>C	ENSP00000493579.1:n.58+100G>C
ENST00000646355.1:c.-21G>C	ENSP00000493801.1:n.-21G>C
ENST00000646590.1:c.58+100G>C	ENSP00000494892.1:n.58+100G>C
ENST00000647335.1:c.-21G>C	ENSP00000495180.1:n.-21G>C
ENST00000256216.10:c.58+100G>C	ENSP00000256216.6:n.58+100G>C
ENST00000442060.7:c.58+100G>C	ENSP00000390208.3:n.58+100G>C
ENST00000504811.5:c.-21G>C	ENSP00000420914.1:n.-21G>C
ENST00000510025.5:c.-80+100G>C	ENSP00000424940.1:n.-80+100G>C
ENST00000511186.5:n.161+100G>C
ENST00000512841.5:n.18G>C
ENST00000515235.6:n.118+100G>C
ENST00000515320.5:c.58+100G>C	ENSP00000424613.1:n.58+100G>C
ENST00000519184.5:n.69+100G>C
NM_000414.3:c.58+100G>C	NP_000405.1:n.58+100G>C
NM_001199291.2:c.-21G>C	NP_001186220.1:n.-21G>C
NM_001199292.1:c.58+100G>C	NP_001186221.1:n.58+100G>C
NM_001292027.1:c.-80+100G>C	NP_001278956.1:n.-80+100G>C
NM_001292028.1:c.-442G>C	NP_001278957.1:n.-442G>C
NM_000414.4:c.58+100G>C MANE Select	NP_000405.1:n.58+100G>C
NM_001199291.3:c.-21G>C	NP_001186220.1:n.-21G>C
NM_001199292.2:c.58+100G>C	NP_001186221.1:n.58+100G>C
NM_001292027.2:c.-80+100G>C	NP_001278956.1:n.-80+100G>C
NM_001292028.2:c.-442G>C	NP_001278957.1:n.-442G>C
NM_001374497.1:c.58+100G>C	NP_001361426.1:n.58+100G>C
NM_001374498.1:c.58+100G>C	NP_001361427.1:n.58+100G>C
NM_001374499.1:c.-376G>C	NP_001361428.1:n.-376G>C
NM_001374500.1:c.-569G>C	NP_001361429.1:n.-569G>C
NM_001374501.1:c.-442G>C	NP_001361430.1:n.-442G>C
NM_001374502.1:c.-447G>C	NP_001361431.1:n.-447G>C
NM_001374503.1:c.-512G>C	NP_001361432.1:n.-512G>C
NR_164653.1:n.137+100G>C
NR_164654.1:n.237G>C