Canonical Allele Identifier: CA1577006812
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119452490C= , CM000667.2:g.119452490C= GRCh38
NC_000005.9:g.118788185C= , CM000667.1:g.118788185C= GRCh37
NC_000005.8:g.118816084C= NCBI36
NG_008182.1:g.5038C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.-86C= ENSP00000426272.2:n.-86C=
ENST00000682996.1:c.-86C= ENSP00000507792.1:n.-86C=
ENST00000683936.1:c.-86C= ENSP00000507721.1:n.-86C=
ENST00000684214.1:c.-86C= ENSP00000508071.1:n.-86C=
ENST00000256216.10:c.-86C= ENSP00000256216.6:n.-86C=
ENST00000511186.5:n.18C=
NM_000414.3:c.-86C= NP_000405.1:n.-86C=
NM_001199292.1:c.-86C= NP_001186221.1:n.-86C=
NM_001292027.1:c.-223C= NP_001278956.1:n.-223C=