Canonical Allele Identifier: CA1577006839

Gene: HSD17B4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.119452521A= , CM000667.2:g.119452521A=	GRCh38
NC_000005.9:g.118788216A= , CM000667.1:g.118788216A=	GRCh37
NC_000005.8:g.118816115A=	NCBI36
NG_008182.1:g.5069A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000509514.6:c.-55A=	ENSP00000426272.2:n.-55A=
ENST00000518349.6:c.-55A=	ENSP00000507185.1:n.-55A=
ENST00000682445.1:c.-55A=	ENSP00000508061.1:n.-55A=
ENST00000682996.1:c.-55A=	ENSP00000507792.1:n.-55A=
ENST00000683936.1:c.-55A=	ENSP00000507721.1:n.-55A=
ENST00000683974.1:n.28A=
ENST00000684214.1:c.-55A=	ENSP00000508071.1:n.-55A=
ENST00000414835.7:c.-233A=	ENSP00000411960.3:n.-233A=
ENST00000510025.7:c.-55A= MANE Select	ENSP00000424940.3:n.-55A=
ENST00000646058.1:c.-55A=	ENSP00000493579.1:n.-55A=
ENST00000646590.1:c.-55A=	ENSP00000494892.1:n.-55A=
ENST00000256216.10:c.-55A=	ENSP00000256216.6:n.-55A=
ENST00000442060.7:c.-55A=	ENSP00000390208.3:n.-55A=
ENST00000511186.5:n.49A=
ENST00000515235.6:n.6A=
ENST00000515320.5:c.-55A=	ENSP00000424613.1:n.-55A=
NM_000414.3:c.-55A=	NP_000405.1:n.-55A=
NM_001199291.2:c.-233A=	NP_001186220.1:n.-233A=
NM_001199292.1:c.-55A=	NP_001186221.1:n.-55A=
NM_001292027.1:c.-192A=	NP_001278956.1:n.-192A=
NM_001292028.1:c.-654A=	NP_001278957.1:n.-654A=
NM_000414.4:c.-55A= MANE Select	NP_000405.1:n.-55A=
NM_001199291.3:c.-233A=	NP_001186220.1:n.-233A=
NM_001199292.2:c.-55A=	NP_001186221.1:n.-55A=
NM_001292027.2:c.-192A=	NP_001278956.1:n.-192A=
NM_001292028.2:c.-654A=	NP_001278957.1:n.-654A=
NM_001374497.1:c.-55A=	NP_001361426.1:n.-55A=
NM_001374498.1:c.-55A=	NP_001361427.1:n.-55A=
NM_001374499.1:c.-588A=	NP_001361428.1:n.-588A=
NM_001374500.1:c.-781A=	NP_001361429.1:n.-781A=
NM_001374501.1:c.-654A=	NP_001361430.1:n.-654A=
NM_001374502.1:c.-659A=	NP_001361431.1:n.-659A=
NM_001374503.1:c.-724A=	NP_001361432.1:n.-724A=
NR_164653.1:n.25A=
NR_164654.1:n.25A=