Canonical Allele Identifier: CA1619250206

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31656191_31656196delinsAGTGTT , CM000668.2:g.31656191_31656196delinsAGTGTT	GRCh38
NC_000006.11:g.31623968_31623973delinsAGTGTT , CM000668.1:g.31623968_31623973delinsAGTGTT	GRCh37
NC_000006.10:g.31731947_31731952delinsAGTGTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.114+111_114+116delinsAGTGTT (APOM) MANE Select	ENSP00000365081.3:n.114+111_114+116delinsAGTGTT
ENST00000375916.3:c.114+111_114+116delinsAGTGTT (APOM)	ENSP00000365081.3:n.114+111_114+116delinsAGTGTT
ENST00000375918.6:c.-102-281_-102-276delinsAGTGTT (APOM)	ENSP00000365083.2:n.-102-281_-102-276delinsAGTGTT
ENST00000375920.8:c.-102-281_-102-276delinsAGTGTT (APOM)	ENSP00000365085.4:n.-102-281_-102-276delinsAGTGTT
NM_001256169.1:c.-102-281_-102-276delinsAGTGTT (APOM)	NP_001243098.1:n.-102-281_-102-276delinsAGTGTT
NM_019101.2:c.114+111_114+116delinsAGTGTT (APOM)	NP_061974.2:n.114+111_114+116delinsAGTGTT
NR_045828.1:n.143-281_143-276delinsAGTGTT (APOM)
XM_006715150.2:c.11+111_11+116delinsAGTGTT (APOM)	XP_006715213.1:n.11+111_11+116delinsAGTGTT
XM_011514895.1:c.-14+4125_-14+4130delinsAACACT (BAG6)	XP_011513197.1:n.-14+4125_-14+4130delinsAACACT
XM_006715150.3:c.11+111_11+116delinsAGTGTT (APOM)	XP_006715213.1:n.11+111_11+116delinsAGTGTT
XM_017011279.2:c.-14+4125_-14+4130delinsAACACT (BAG6)	XP_016866768.1:n.-14+4125_-14+4130delinsAACACT
XM_024446545.1:c.-14+1568_-14+1573delinsAACACT (BAG6)	XP_024302313.1:n.-14+1568_-14+1573delinsAACACT
NM_019101.3:c.114+111_114+116delinsAGTGTT (APOM) MANE Select	NP_061974.2:n.114+111_114+116delinsAGTGTT
NM_001256169.2:c.-102-281_-102-276delinsAGTGTT (APOM)	NP_001243098.1:n.-102-281_-102-276delinsAGTGTT
NR_045828.2:n.149-281_149-276delinsAGTGTT (APOM)