Canonical Allele Identifier: CA527135199

Gene: APOA2

Linked Data

• dbSNP Id: rs1274208727
• gnomAD v2: 1-161192133-TA-T
• gnomAD v3: 1-161222343-TA-T
• gnomAD v4: 1-161222343-TA-T
• MyVariant Identifiers: chr1:g.161192134del (hg19) ; chr1:g.161222344del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222344del , CM000663.2:g.161222344del	GRCh38
NC_000001.10:g.161192134del , CM000663.1:g.161192134del	GRCh37
NC_000001.9:g.159458758del	NCBI36
NG_012043.1:g.6285del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.*61del MANE Select	ENSP00000356969.3:n.*61del
ENST00000463812.1:c.*61del	ENSP00000476890.1:n.*61del
ENST00000464492.5:c.*61del	ENSP00000476911.1:n.*61del
ENST00000468465.5:c.*61del	ENSP00000476662.1:n.*61del
ENST00000470459.6:c.*61del	ENSP00000477031.1:n.*61del
ENST00000481413.1:n.875del
ENST00000481511.5:c.*361del	ENSP00000477054.1:n.*361del
ENST00000491350.1:c.*147del	ENSP00000477353.1:n.*147del
NM_001643.1:c.*61del	NP_001634.1:n.*61del
NM_001643.2:c.*61del MANE Select	NP_001634.1:n.*61del