Canonical Allele Identifier: CA2271191741

Gene: APOH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66227933_66227936delinsACTC , CM000679.2:g.66227933_66227936delinsACTC	GRCh38
NC_000017.10:g.64224051_64224054delinsACTC , CM000679.1:g.64224051_64224054delinsACTC	GRCh37
NC_000017.9:g.61654513_61654516delinsACTC	NCBI36
NG_012045.1:g.6503_6506delinsGAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205948.11:c.241+84_241+87delinsGAGT MANE Select	ENSP00000205948.6:n.241+84_241+87delinsGAGT
ENST00000205948.10:c.241+84_241+87delinsGAGT	ENSP00000205948.6:n.241+84_241+87delinsGAGT
ENST00000577982.1:c.241+84_241+87delinsGAGT	ENSP00000464301.1:n.241+84_241+87delinsGAGT
ENST00000581797.5:c.61+84_61+87delinsGAGT	ENSP00000463553.1:n.61+84_61+87delinsGAGT
NM_000042.2:c.241+84_241+87delinsGAGT	NP_000033.2:n.241+84_241+87delinsGAGT
NM_000042.3:c.241+84_241+87delinsGAGT MANE Select	NP_000033.2:n.241+84_241+87delinsGAGT