Canonical Allele Identifier: CA1967710553
Gene: HSD17B12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.43706872_43706878delinsGCAAGTA , CM000673.2:g.43706872_43706878delinsGCAAGTA GRCh38
NC_000011.9:g.43728422_43728428delinsGCAAGTA , CM000673.1:g.43728422_43728428delinsGCAAGTA GRCh37
NC_000011.8:g.43684998_43685004delinsGCAAGTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000278353.10:c.160+25885_160+25891delinsGCAAGTA MANE Select ENSP00000278353.4:n.160+25885_160+25891delinsGCAAGTA
ENST00000527433.6:c.123+26068_123+26074delinsGCAAGTA ENSP00000490749.1:n.123+26068_123+26074delinsGCAAGTA
ENST00000636007.1:c.160+25885_160+25891delinsGCAAGTA ENSP00000490822.1:n.160+25885_160+25891delinsGCAAGTA
ENST00000636722.1:c.*20+25689_*20+25695delinsGCAAGTA ENSP00000490003.1:n.*20+25689_*20+25695delinsGCAAGTA
ENST00000637401.1:c.160+25885_160+25891delinsGCAAGTA ENSP00000490421.1:n.160+25885_160+25891delinsGCAAGTA
ENST00000638034.1:c.64+25515_64+25521delinsGCAAGTA ENSP00000490701.1:n.64+25515_64+25521delinsGCAAGTA
ENST00000278353.8:c.160+25885_160+25891delinsGCAAGTA ENSP00000278353.4:n.160+25885_160+25891delinsGCAAGTA
ENST00000395700.4:c.160+25885_160+25891delinsGCAAGTA ENSP00000379052.4:n.160+25885_160+25891delinsGCAAGTA
ENST00000527433.5:n.125+26068_125+26074delinsGCAAGTA
ENST00000529261.5:n.377+33733_377+33739delinsGCAAGTA
ENST00000531185.5:c.160+25885_160+25891delinsGCAAGTA ENSP00000436582.1:n.160+25885_160+25891delinsGCAAGTA
ENST00000532864.5:n.282-44039_282-44033delinsGCAAGTA
NM_016142.2:c.160+25885_160+25891delinsGCAAGTA NP_057226.1:n.160+25885_160+25891delinsGCAAGTA
XM_011520156.1:c.-63+25689_-63+25695delinsGCAAGTA XP_011518458.1:n.-63+25689_-63+25695delinsGCAAGTA
XM_017017881.1:c.64+25515_64+25521delinsGCAAGTA XP_016873370.1:n.64+25515_64+25521delinsGCAAGTA
XM_024448571.1:c.-62-44039_-62-44033delinsGCAAGTA XP_024304339.1:n.-62-44039_-62-44033delinsGCAAGTA
XM_024448572.1:c.-62-44039_-62-44033delinsGCAAGTA XP_024304340.1:n.-62-44039_-62-44033delinsGCAAGTA
XM_024448573.1:c.-62-44039_-62-44033delinsGCAAGTA XP_024304341.1:n.-62-44039_-62-44033delinsGCAAGTA
NM_016142.3:c.160+25885_160+25891delinsGCAAGTA MANE Select NP_057226.1:n.160+25885_160+25891delinsGCAAGTA