Canonical Allele Identifier: CA221900299
Gene: HSD17B12 HGNC NCBI

Linked Data

dbSNP Id: rs898178208

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.43706824_43706835del , CM000673.2:g.43706824_43706835del GRCh38
NC_000011.9:g.43728374_43728385del , CM000673.1:g.43728374_43728385del GRCh37
NC_000011.8:g.43684950_43684961del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000278353.10:c.160+25837_160+25848del MANE Select ENSP00000278353.4:n.160+25837_160+25848del
ENST00000527433.6:c.123+26020_123+26031del ENSP00000490749.1:n.123+26020_123+26031del
ENST00000636007.1:c.160+25837_160+25848del ENSP00000490822.1:n.160+25837_160+25848del
ENST00000636722.1:c.*20+25641_*20+25652del ENSP00000490003.1:n.*20+25641_*20+25652del
ENST00000637401.1:c.160+25837_160+25848del ENSP00000490421.1:n.160+25837_160+25848del
ENST00000638034.1:c.64+25467_64+25478del ENSP00000490701.1:n.64+25467_64+25478del
ENST00000278353.8:c.160+25837_160+25848del ENSP00000278353.4:n.160+25837_160+25848del
ENST00000395700.4:c.160+25837_160+25848del ENSP00000379052.4:n.160+25837_160+25848del
ENST00000527433.5:n.125+26020_125+26031del
ENST00000529261.5:n.377+33685_377+33696del
ENST00000531185.5:c.160+25837_160+25848del ENSP00000436582.1:n.160+25837_160+25848del
ENST00000532864.5:n.282-44087_282-44076del
NM_016142.2:c.160+25837_160+25848del NP_057226.1:n.160+25837_160+25848del
XM_011520156.1:c.-63+25641_-63+25652del XP_011518458.1:n.-63+25641_-63+25652del
XM_017017881.1:c.64+25467_64+25478del XP_016873370.1:n.64+25467_64+25478del
XM_024448571.1:c.-62-44087_-62-44076del XP_024304339.1:n.-62-44087_-62-44076del
XM_024448572.1:c.-62-44087_-62-44076del XP_024304340.1:n.-62-44087_-62-44076del
XM_024448573.1:c.-62-44087_-62-44076del XP_024304341.1:n.-62-44087_-62-44076del
NM_016142.3:c.160+25837_160+25848del MANE Select NP_057226.1:n.160+25837_160+25848del