Canonical Allele Identifier: CA1202652344

Gene: APOA2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222501_161222502delinsCT , CM000663.2:g.161222501_161222502delinsCT	GRCh38
NC_000001.10:g.161192291_161192292delinsCT , CM000663.1:g.161192291_161192292delinsCT	GRCh37
NC_000001.9:g.159458915_159458916delinsCT	NCBI36
NG_012043.1:g.6127_6128delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.206_207delinsAG MANE Select	ENSP00000356969.3:p.Lys69=
ENST00000463273.5:c.206_207delinsAG	ENSP00000476740.1:p.Lys69=
ENST00000463812.1:c.62_63delinsAG	ENSP00000476890.1:p.Lys21=
ENST00000464492.5:c.305_306delinsAG	ENSP00000476911.1:p.Lys102=
ENST00000468465.5:c.62_63delinsAG	ENSP00000476662.1:p.Lys21=
ENST00000470459.6:c.200+6_200+7delinsAG	ENSP00000477031.1:n.200+6_200+7delinsAG
ENST00000481413.1:n.717_718delinsAG
ENST00000481511.5:c.*203_*204delinsAG	ENSP00000477054.1:n.*203_*204delinsAG
ENST00000491350.1:c.73_74delinsAG	ENSP00000477353.1:p.Arg25=
NM_001643.1:c.206_207delinsAG	NP_001634.1:p.Lys69=
NM_001643.2:c.206_207delinsAG MANE Select	NP_001634.1:p.Lys69=