Canonical Allele Identifier: CA2810190838

Gene: APOH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66228271_66228272insCCAAACACACCCAACAC , CM000679.2:g.66228271_66228272insCCAAACACACCCAACAC	GRCh38
NC_000017.10:g.64224389_64224390insCCAAACACACCCAACAC , CM000679.1:g.64224389_64224390insCCAAACACACCCAACAC	GRCh37
NC_000017.9:g.61654851_61654852insCCAAACACACCCAACAC	NCBI36
NG_012045.1:g.6167_6168insGTGTTGGGTGTGTTTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205948.11:c.65-76_65-75insGTGTTGGGTGTGTTTGG MANE Select	ENSP00000205948.6:n.65-76_65-75insGTGTTGGGTGTGTTTGG
ENST00000205948.10:c.65-76_65-75insGTGTTGGGTGTGTTTGG	ENSP00000205948.6:n.65-76_65-75insGTGTTGGGTGTGTTTGG
ENST00000577982.1:c.65-76_65-75insGTGTTGGGTGTGTTTGG	ENSP00000464301.1:n.65-76_65-75insGTGTTGGGTGTGTTTGG
ENST00000581797.5:c.-116-76_-116-75insGTGTTGGGTGTGTTTGG	ENSP00000463553.1:n.-116-76_-116-75insGTGTTGGGTGTGTTTGG
NM_000042.2:c.65-76_65-75insGTGTTGGGTGTGTTTGG	NP_000033.2:n.65-76_65-75insGTGTTGGGTGTGTTTGG
NM_000042.3:c.65-76_65-75insGTGTTGGGTGTGTTTGG MANE Select	NP_000033.2:n.65-76_65-75insGTGTTGGGTGTGTTTGG