Canonical Allele Identifier: CA2271191895
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228259_66228260delinsGC , CM000679.2:g.66228259_66228260delinsGC GRCh38
NC_000017.10:g.64224377_64224378delinsGC , CM000679.1:g.64224377_64224378delinsGC GRCh37
NC_000017.9:g.61654839_61654840delinsGC NCBI36
NG_012045.1:g.6179_6180delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.65-64_65-63delinsGC MANE Select ENSP00000205948.6:n.65-64_65-63delinsGC
ENST00000205948.10:c.65-64_65-63delinsGC ENSP00000205948.6:n.65-64_65-63delinsGC
ENST00000577982.1:c.65-64_65-63delinsGC ENSP00000464301.1:n.65-64_65-63delinsGC
ENST00000581797.5:c.-116-64_-116-63delinsGC ENSP00000463553.1:n.-116-64_-116-63delinsGC
NM_000042.2:c.65-64_65-63delinsGC NP_000033.2:n.65-64_65-63delinsGC
NM_000042.3:c.65-64_65-63delinsGC MANE Select NP_000033.2:n.65-64_65-63delinsGC