Canonical Allele Identifier: CA2002741011

Gene: APOA5

Linked Data

• dbSNP Id: rs1940996317

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116790866del , CM000673.2:g.116790866del	GRCh38
NC_000011.9:g.116661582del , CM000673.1:g.116661582del	GRCh37
NC_000011.8:g.116166792del	NCBI36
NG_015894.1:g.6557del
NG_015894.2:g.6557del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.365del MANE Select	ENSP00000227665.4:p.Leu122TrpfsTer8
ENST00000433069.2:c.365del	ENSP00000399701.2:p.Leu122TrpfsTer8
ENST00000673688.1:c.449del	ENSP00000501141.1:p.Leu150TrpfsTer8
ENST00000227665.8:c.365del	ENSP00000227665.4:p.Leu122TrpfsTer8
ENST00000433069.1:c.365del	ENSP00000399701.1:p.Leu122TrpfsTer8
ENST00000542499.5:c.365del	ENSP00000445002.1:p.Leu122TrpfsTer8
NM_001166598.1:c.365del	NP_001160070.1:p.Leu122TrpfsTer8
NM_052968.4:c.365del	NP_443200.2:p.Leu122TrpfsTer8
NM_001166598.2:c.365del	NP_001160070.1:p.Leu122TrpfsTer8
NM_001371904.1:c.365del MANE Select	NP_001358833.1:p.Leu122TrpfsTer8
NM_052968.5:c.365del	NP_443200.2:p.Leu122TrpfsTer8