Canonical Allele Identifier: CA676707286

Gene: HSD17B12

Linked Data

• dbSNP Id: rs1415184752
• MyVariant Identifiers: chr11:g.43728237_43728238insGTGTGTGTGTGT (hg19) ; chr11:g.43706687_43706688insGTGTGTGTGTGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.43706688_43706689insTGTGTGTGTGTG , CM000673.2:g.43706688_43706689insTGTGTGTGTGTG	GRCh38
NC_000011.9:g.43728238_43728239insTGTGTGTGTGTG , CM000673.1:g.43728238_43728239insTGTGTGTGTGTG	GRCh37
NC_000011.8:g.43684814_43684815insTGTGTGTGTGTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278353.10:c.160+25701_160+25702insTGTGTGTGTGTG MANE Select	ENSP00000278353.4:n.160+25701_160+25702insTGTGTGTGTGTG
ENST00000527433.6:c.123+25884_123+25885insTGTGTGTGTGTG	ENSP00000490749.1:n.123+25884_123+25885insTGTGTGTGTGTG
ENST00000636007.1:c.160+25701_160+25702insTGTGTGTGTGTG	ENSP00000490822.1:n.160+25701_160+25702insTGTGTGTGTGTG
ENST00000636722.1:c.*20+25505_*20+25506insTGTGTGTGTGTG	ENSP00000490003.1:n.*20+25505_*20+25506insTGTGTGTGTGTG
ENST00000637401.1:c.160+25701_160+25702insTGTGTGTGTGTG	ENSP00000490421.1:n.160+25701_160+25702insTGTGTGTGTGTG
ENST00000638034.1:c.64+25331_64+25332insTGTGTGTGTGTG	ENSP00000490701.1:n.64+25331_64+25332insTGTGTGTGTGTG
ENST00000278353.8:c.160+25701_160+25702insTGTGTGTGTGTG	ENSP00000278353.4:n.160+25701_160+25702insTGTGTGTGTGTG
ENST00000395700.4:c.160+25701_160+25702insTGTGTGTGTGTG	ENSP00000379052.4:n.160+25701_160+25702insTGTGTGTGTGTG
ENST00000527433.5:n.125+25884_125+25885insTGTGTGTGTGTG
ENST00000529261.5:n.377+33549_377+33550insTGTGTGTGTGTG
ENST00000531185.5:c.160+25701_160+25702insTGTGTGTGTGTG	ENSP00000436582.1:n.160+25701_160+25702insTGTGTGTGTGTG
ENST00000532864.5:n.282-44223_282-44222insTGTGTGTGTGTG
NM_016142.2:c.160+25701_160+25702insTGTGTGTGTGTG	NP_057226.1:n.160+25701_160+25702insTGTGTGTGTGTG
XM_011520156.1:c.-63+25505_-63+25506insTGTGTGTGTGTG	XP_011518458.1:n.-63+25505_-63+25506insTGTGTGTGTGTG
XM_017017881.1:c.64+25331_64+25332insTGTGTGTGTGTG	XP_016873370.1:n.64+25331_64+25332insTGTGTGTGTGTG
XM_024448571.1:c.-62-44223_-62-44222insTGTGTGTGTGTG	XP_024304339.1:n.-62-44223_-62-44222insTGTGTGTGTGTG
XM_024448572.1:c.-62-44223_-62-44222insTGTGTGTGTGTG	XP_024304340.1:n.-62-44223_-62-44222insTGTGTGTGTGTG
XM_024448573.1:c.-62-44223_-62-44222insTGTGTGTGTGTG	XP_024304341.1:n.-62-44223_-62-44222insTGTGTGTGTGTG
NM_016142.3:c.160+25701_160+25702insTGTGTGTGTGTG MANE Select	NP_057226.1:n.160+25701_160+25702insTGTGTGTGTGTG