Canonical Allele Identifier: CA2648766618

Gene: APOA2

Linked Data

• gnomAD v4: 1-161222786-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222791del , CM000663.2:g.161222791del	GRCh38
NC_000001.10:g.161192581del , CM000663.1:g.161192581del	GRCh37
NC_000001.9:g.159459205del	NCBI36
NG_012043.1:g.5842del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.185+131del MANE Select	ENSP00000356969.3:n.185+131del
ENST00000463273.5:c.185+131del	ENSP00000476740.1:n.185+131del
ENST00000463812.1:c.41+131del	ENSP00000476890.1:n.41+131del
ENST00000464492.5:c.284+131del	ENSP00000476911.1:n.284+131del
ENST00000468465.5:c.41+131del	ENSP00000476662.1:n.41+131del
ENST00000469730.2:c.185+131del	ENSP00000476605.1:n.185+131del
ENST00000470459.6:c.185+131del	ENSP00000477031.1:n.185+131del
ENST00000481413.1:n.696+131del
ENST00000481511.5:c.*182+131del	ENSP00000477054.1:n.*182+131del
ENST00000491350.1:c.53-265del	ENSP00000477353.1:n.53-265del
NM_001643.1:c.185+131del	NP_001634.1:n.185+131del
NM_001643.2:c.185+131del MANE Select	NP_001634.1:n.185+131del