Canonical Allele Identifier: CA1967710367
Gene: HSD17B12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.43706784G= , CM000673.2:g.43706784G= GRCh38
NC_000011.9:g.43728334G= , CM000673.1:g.43728334G= GRCh37
NC_000011.8:g.43684910G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000278353.10:c.160+25797G= MANE Select ENSP00000278353.4:n.160+25797G=
ENST00000527433.6:c.123+25980G= ENSP00000490749.1:n.123+25980G=
ENST00000636007.1:c.160+25797G= ENSP00000490822.1:n.160+25797G=
ENST00000636722.1:c.*20+25601G= ENSP00000490003.1:n.*20+25601G=
ENST00000637401.1:c.160+25797G= ENSP00000490421.1:n.160+25797G=
ENST00000638034.1:c.64+25427G= ENSP00000490701.1:n.64+25427G=
ENST00000278353.8:c.160+25797G= ENSP00000278353.4:n.160+25797G=
ENST00000395700.4:c.160+25797G= ENSP00000379052.4:n.160+25797G=
ENST00000527433.5:n.125+25980G=
ENST00000529261.5:n.377+33645G=
ENST00000531185.5:c.160+25797G= ENSP00000436582.1:n.160+25797G=
ENST00000532864.5:n.282-44127G=
NM_016142.2:c.160+25797G= NP_057226.1:n.160+25797G=
XM_011520156.1:c.-63+25601G= XP_011518458.1:n.-63+25601G=
XM_017017881.1:c.64+25427G= XP_016873370.1:n.64+25427G=
XM_024448571.1:c.-62-44127G= XP_024304339.1:n.-62-44127G=
XM_024448572.1:c.-62-44127G= XP_024304340.1:n.-62-44127G=
XM_024448573.1:c.-62-44127G= XP_024304341.1:n.-62-44127G=
NM_016142.3:c.160+25797G= MANE Select NP_057226.1:n.160+25797G=