Canonical Allele Identifier: CA1967710444

Gene: HSD17B12

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.43706821_43706833delinsGTATTATGCTGAC , CM000673.2:g.43706821_43706833delinsGTATTATGCTGAC	GRCh38
NC_000011.9:g.43728371_43728383delinsGTATTATGCTGAC , CM000673.1:g.43728371_43728383delinsGTATTATGCTGAC	GRCh37
NC_000011.8:g.43684947_43684959delinsGTATTATGCTGAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278353.10:c.160+25834_160+25846delinsGTATTATGCTGAC MANE Select	ENSP00000278353.4:n.160+25834_160+25846delinsGTATTATGCTGAC
ENST00000527433.6:c.123+26017_123+26029delinsGTATTATGCTGAC	ENSP00000490749.1:n.123+26017_123+26029delinsGTATTATGCTGAC
ENST00000636007.1:c.160+25834_160+25846delinsGTATTATGCTGAC	ENSP00000490822.1:n.160+25834_160+25846delinsGTATTATGCTGAC
ENST00000636722.1:c.*20+25638_*20+25650delinsGTATTATGCTGAC	ENSP00000490003.1:n.*20+25638_*20+25650delinsGTATTATGCTGAC
ENST00000637401.1:c.160+25834_160+25846delinsGTATTATGCTGAC	ENSP00000490421.1:n.160+25834_160+25846delinsGTATTATGCTGAC
ENST00000638034.1:c.64+25464_64+25476delinsGTATTATGCTGAC	ENSP00000490701.1:n.64+25464_64+25476delinsGTATTATGCTGAC
ENST00000278353.8:c.160+25834_160+25846delinsGTATTATGCTGAC	ENSP00000278353.4:n.160+25834_160+25846delinsGTATTATGCTGAC
ENST00000395700.4:c.160+25834_160+25846delinsGTATTATGCTGAC	ENSP00000379052.4:n.160+25834_160+25846delinsGTATTATGCTGAC
ENST00000527433.5:n.125+26017_125+26029delinsGTATTATGCTGAC
ENST00000529261.5:n.377+33682_377+33694delinsGTATTATGCTGAC
ENST00000531185.5:c.160+25834_160+25846delinsGTATTATGCTGAC	ENSP00000436582.1:n.160+25834_160+25846delinsGTATTATGCTGAC
ENST00000532864.5:n.282-44090_282-44078delinsGTATTATGCTGAC
NM_016142.2:c.160+25834_160+25846delinsGTATTATGCTGAC	NP_057226.1:n.160+25834_160+25846delinsGTATTATGCTGAC
XM_011520156.1:c.-63+25638_-63+25650delinsGTATTATGCTGAC	XP_011518458.1:n.-63+25638_-63+25650delinsGTATTATGCTGAC
XM_017017881.1:c.64+25464_64+25476delinsGTATTATGCTGAC	XP_016873370.1:n.64+25464_64+25476delinsGTATTATGCTGAC
XM_024448571.1:c.-62-44090_-62-44078delinsGTATTATGCTGAC	XP_024304339.1:n.-62-44090_-62-44078delinsGTATTATGCTGAC
XM_024448572.1:c.-62-44090_-62-44078delinsGTATTATGCTGAC	XP_024304340.1:n.-62-44090_-62-44078delinsGTATTATGCTGAC
XM_024448573.1:c.-62-44090_-62-44078delinsGTATTATGCTGAC	XP_024304341.1:n.-62-44090_-62-44078delinsGTATTATGCTGAC
NM_016142.3:c.160+25834_160+25846delinsGTATTATGCTGAC MANE Select	NP_057226.1:n.160+25834_160+25846delinsGTATTATGCTGAC