Canonical Allele Identifier: CA382738141

Gene: APOA5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116790676C>G , CM000673.2:g.116790676C>G	GRCh38
NC_000011.9:g.116661392C>G , CM000673.1:g.116661392C>G	GRCh37
NC_000011.8:g.116166602C>G	NCBI36
NG_015894.1:g.6745G>C
NG_015894.2:g.6745G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001371904.1:c.553G>C MANE Select	NP_001358833.1:p.Gly185Arg
ENST00000227665.9:c.553G>C MANE Select	ENSP00000227665.4:p.Gly185Arg
NM_001166598.1:c.553G>C	NP_001160070.1:p.Gly185Arg
NM_001166598.2:c.553G>C	NP_001160070.1:p.Gly185Arg
NM_052968.4:c.553G>C	NP_443200.2:p.Gly185Arg
NM_052968.5:c.553G>C	NP_443200.2:p.Gly185Arg
ENST00000227665.8:c.553G>C	ENSP00000227665.4:p.Gly185Arg
ENST00000433069.2:c.553G>C	ENSP00000399701.2:p.Gly185Arg
ENST00000542499.5:c.553G>C	ENSP00000445002.1:p.Gly185Arg
ENST00000673688.1:c.637G>C	ENSP00000501141.1:p.Gly213Arg