Canonical Allele Identifier: CA2578387461

Gene: HSD17B4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.119479081T>C , CM000667.2:g.119479081T>C	GRCh38
NC_000005.9:g.118814776T>C , CM000667.1:g.118814776T>C	GRCh37
NC_000005.8:g.118842675T>C	NCBI36
NG_008182.1:g.31629T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509514.6:c.622+60T>C	ENSP00000426272.2:n.622+60T>C
ENST00000518349.6:c.113-17462T>C	ENSP00000507185.1:n.113-17462T>C
ENST00000682445.1:c.*503+60T>C	ENSP00000508061.1:n.*503+60T>C
ENST00000682531.1:n.723+60T>C
ENST00000682626.1:c.*128+60T>C	ENSP00000507857.1:n.*128+60T>C
ENST00000682996.1:c.622+60T>C	ENSP00000507792.1:n.622+60T>C
ENST00000683265.1:n.715+60T>C
ENST00000683371.1:c.*752+60T>C	ENSP00000508376.1:n.*752+60T>C
ENST00000683390.1:n.2312+60T>C
ENST00000683549.1:n.543+60T>C
ENST00000683936.1:c.*507+60T>C	ENSP00000507721.1:n.*507+60T>C
ENST00000683974.1:n.704+60T>C
ENST00000683996.1:c.211+60T>C	ENSP00000507060.1:n.211+60T>C
ENST00000684131.1:n.461+60T>C
ENST00000684160.1:c.*312+60T>C	ENSP00000507821.1:n.*312+60T>C
ENST00000684214.1:c.622+60T>C	ENSP00000508071.1:n.622+60T>C
ENST00000414835.7:c.697+60T>C	ENSP00000411960.3:n.697+60T>C
ENST00000510025.7:c.622+60T>C MANE Select	ENSP00000424940.3:n.622+60T>C
ENST00000643250.1:c.*494+60T>C	ENSP00000494737.1:n.*494+60T>C
ENST00000644146.1:c.*200+60T>C	ENSP00000494808.1:n.*200+60T>C
ENST00000645099.1:c.181+60T>C	ENSP00000496091.1:n.181+60T>C
ENST00000645702.1:c.211+60T>C	ENSP00000496432.1:n.211+60T>C
ENST00000645832.1:c.*507+60T>C	ENSP00000494316.1:n.*507+60T>C
ENST00000646058.1:c.622+60T>C	ENSP00000493579.1:n.622+60T>C
ENST00000646355.1:c.*628+60T>C	ENSP00000493801.1:n.*628+60T>C
ENST00000646554.1:c.*600+60T>C	ENSP00000494542.1:n.*600+60T>C
ENST00000647335.1:c.*589+60T>C	ENSP00000495180.1:n.*589+60T>C
ENST00000647342.1:c.*553+60T>C	ENSP00000494992.1:n.*553+60T>C
ENST00000256216.10:c.622+60T>C	ENSP00000256216.6:n.622+60T>C
ENST00000414835.6:c.202+60T>C	ENSP00000411960.2:n.202+60T>C
ENST00000442060.7:c.622+60T>C	ENSP00000390208.3:n.622+60T>C
ENST00000504811.5:c.697+60T>C	ENSP00000420914.1:n.697+60T>C
ENST00000505181.5:n.325+60T>C
ENST00000509514.5:c.-263+60T>C	ENSP00000426272.1:n.-263+60T>C
ENST00000510025.5:c.550+60T>C	ENSP00000424940.1:n.550+60T>C
ENST00000512644.1:n.190+60T>C
ENST00000513628.5:c.211+60T>C	ENSP00000425993.1:n.211+60T>C
ENST00000515235.6:n.682+60T>C
ENST00000515320.5:c.568+60T>C	ENSP00000424613.1:n.568+60T>C
NM_000414.3:c.622+60T>C	NP_000405.1:n.622+60T>C
NM_001199291.2:c.697+60T>C	NP_001186220.1:n.697+60T>C
NM_001199292.1:c.568+60T>C	NP_001186221.1:n.568+60T>C
NM_001292027.1:c.550+60T>C	NP_001278956.1:n.550+60T>C
NM_001292028.1:c.202+60T>C	NP_001278957.1:n.202+60T>C
NM_000414.4:c.622+60T>C MANE Select	NP_000405.1:n.622+60T>C
NM_001199291.3:c.697+60T>C	NP_001186220.1:n.697+60T>C
NM_001199292.2:c.568+60T>C	NP_001186221.1:n.568+60T>C
NM_001292027.2:c.550+60T>C	NP_001278956.1:n.550+60T>C
NM_001292028.2:c.202+60T>C	NP_001278957.1:n.202+60T>C
NM_001374497.1:c.613+60T>C	NP_001361426.1:n.613+60T>C
NM_001374498.1:c.622+60T>C	NP_001361427.1:n.622+60T>C
NM_001374499.1:c.295+60T>C	NP_001361428.1:n.295+60T>C
NM_001374500.1:c.181+60T>C	NP_001361429.1:n.181+60T>C
NM_001374501.1:c.211+60T>C	NP_001361430.1:n.211+60T>C
NM_001374502.1:c.211+60T>C	NP_001361431.1:n.211+60T>C
NM_001374503.1:c.211+60T>C	NP_001361432.1:n.211+60T>C
NR_164653.1:n.701+60T>C
NR_164654.1:n.889+60T>C