Canonical Allele Identifier: CA406311196
Gene: APOC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44919206G>C , CM000681.2:g.44919206G>C GRCh38
NC_000019.9:g.45422463G>C , CM000681.1:g.45422463G>C GRCh37
NC_000019.8:g.50114303G>C NCBI36
NG_012859.1:g.9543G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000592535.6:c.228G>C MANE Select ENSP00000468276.2:p.Lys76Asn
ENST00000586638.5:c.262G>C ENSP00000466146.1:p.Gly88Arg
ENST00000588750.5:c.228G>C ENSP00000465356.1:p.Lys76Asn
ENST00000588802.5:c.228G>C ENSP00000468029.1:p.Lys76Asn
ENST00000589781.1:c.*2G>C ENSP00000467504.1:n.*2G>C
ENST00000590334.5:c.*97G>C ENSP00000465190.1:n.*97G>C
ENST00000592176.1:c.*228G>C ENSP00000466227.1:n.*228G>C
ENST00000592535.5:c.228G>C ENSP00000468276.1:p.Lys76Asn
ENST00000592885.5:c.373G>C ENSP00000467368.1:p.Gly125Arg
NM_001645.3:c.228G>C NP_001636.1:p.Lys76Asn
XM_005258855.2:c.228G>C XP_005258912.1:p.Lys76Asn
NM_001321065.1:c.228G>C NP_001307994.1:p.Lys76Asn
NM_001321066.1:c.228G>C NP_001307995.1:p.Lys76Asn
NM_001645.4:c.228G>C NP_001636.1:p.Lys76Asn
NM_001321065.2:c.228G>C NP_001307994.1:p.Lys76Asn
NM_001321066.2:c.228G>C NP_001307995.1:p.Lys76Asn
NM_001645.5:c.228G>C MANE Select NP_001636.1:p.Lys76Asn
NM_001379687.1:c.373G>C NP_001366616.1:p.Gly125Arg