Canonical Allele Identifier: CA382738145

Gene: APOA5

Linked Data

• dbSNP Id: rs201229911
• gnomAD v2: 11-116661394-G-A
• gnomAD v3: 11-116790678-G-A
• gnomAD v4: 11-116790678-G-A
• MyVariant Identifiers: chr11:g.116661394G>A (hg19) ; chr11:g.116790678G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116790678G>A , CM000673.2:g.116790678G>A	GRCh38
NC_000011.9:g.116661394G>A , CM000673.1:g.116661394G>A	GRCh37
NC_000011.8:g.116166604G>A	NCBI36
NG_015894.1:g.6743C>T
NG_015894.2:g.6743C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.551C>T MANE Select	ENSP00000227665.4:p.Thr184Ile
ENST00000433069.2:c.551C>T	ENSP00000399701.2:p.Thr184Ile
ENST00000673688.1:c.635C>T	ENSP00000501141.1:p.Thr212Ile
ENST00000227665.8:c.551C>T	ENSP00000227665.4:p.Thr184Ile
ENST00000542499.5:c.551C>T	ENSP00000445002.1:p.Thr184Ile
NM_001166598.1:c.551C>T	NP_001160070.1:p.Thr184Ile
NM_052968.4:c.551C>T	NP_443200.2:p.Thr184Ile
NM_001166598.2:c.551C>T	NP_001160070.1:p.Thr184Ile
NM_001371904.1:c.551C>T MANE Select	NP_001358833.1:p.Thr184Ile
NM_052968.5:c.551C>T	NP_443200.2:p.Thr184Ile