Canonical Allele Identifier: CA2338173498

Gene: APOC1

Linked Data

• dbSNP Id: rs12721054
• gnomAD v4: 19-44919330-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44919330A>C , CM000681.2:g.44919330A>C	GRCh38
NC_000019.9:g.45422587A>C , CM000681.1:g.45422587A>C	GRCh37
NC_000019.8:g.50114427A>C	NCBI36
NG_012859.1:g.9667A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000592535.6:c.*100A>C MANE Select	ENSP00000468276.2:n.*100A>C
ENST00000586638.5:c.*107A>C	ENSP00000466146.1:n.*107A>C
ENST00000588750.5:c.*100A>C	ENSP00000465356.1:n.*100A>C
ENST00000588802.5:c.*100A>C	ENSP00000468029.1:n.*100A>C
ENST00000589781.1:c.*126A>C	ENSP00000467504.1:n.*126A>C
ENST00000590334.5:c.*221A>C	ENSP00000465190.1:n.*221A>C
ENST00000592176.1:c.*352A>C	ENSP00000466227.1:n.*352A>C
ENST00000592885.5:c.*107A>C	ENSP00000467368.1:n.*107A>C
NM_001645.3:c.*100A>C	NP_001636.1:n.*100A>C
XM_005258855.2:c.*100A>C	XP_005258912.1:n.*100A>C
NM_001321065.1:c.*100A>C	NP_001307994.1:n.*100A>C
NM_001321066.1:c.*100A>C	NP_001307995.1:n.*100A>C
NM_001645.4:c.*100A>C	NP_001636.1:n.*100A>C
NM_001321065.2:c.*100A>C	NP_001307994.1:n.*100A>C
NM_001321066.2:c.*100A>C	NP_001307995.1:n.*100A>C
NM_001645.5:c.*100A>C MANE Select	NP_001636.1:n.*100A>C
NM_001379687.1:c.*107A>C	NP_001366616.1:n.*107A>C