Canonical Allele Identifier: CA2639419335
Gene: APOH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228268_66228269del , CM000679.2:g.66228268_66228269del GRCh38
NC_000017.10:g.64224386_64224387del , CM000679.1:g.64224386_64224387del GRCh37
NC_000017.9:g.61654848_61654849del NCBI36
NG_012045.1:g.6170_6171del

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.65-73_65-72del MANE Select ENSP00000205948.6:n.65-73_65-72del
ENST00000205948.10:c.65-73_65-72del ENSP00000205948.6:n.65-73_65-72del
ENST00000577982.1:c.65-73_65-72del ENSP00000464301.1:n.65-73_65-72del
ENST00000581797.5:c.-116-73_-116-72del ENSP00000463553.1:n.-116-73_-116-72del
NM_000042.2:c.65-73_65-72del NP_000033.2:n.65-73_65-72del
NM_000042.3:c.65-73_65-72del MANE Select NP_000033.2:n.65-73_65-72del