Canonical Allele Identifier: CA1619250260

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31656327_31656329delinsCTT , CM000668.2:g.31656327_31656329delinsCTT	GRCh38
NC_000006.11:g.31624104_31624106delinsCTT , CM000668.1:g.31624104_31624106delinsCTT	GRCh37
NC_000006.10:g.31732083_31732085delinsCTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.115-145_115-143delinsCTT (APOM) MANE Select	ENSP00000365081.3:n.115-145_115-143delinsCTT
ENST00000375916.3:c.115-145_115-143delinsCTT (APOM)	ENSP00000365081.3:n.115-145_115-143delinsCTT
ENST00000375918.6:c.-102-145_-102-143delinsCTT (APOM)	ENSP00000365083.2:n.-102-145_-102-143delinsCTT
ENST00000375920.8:c.-102-145_-102-143delinsCTT (APOM)	ENSP00000365085.4:n.-102-145_-102-143delinsCTT
NM_001256169.1:c.-102-145_-102-143delinsCTT (APOM)	NP_001243098.1:n.-102-145_-102-143delinsCTT
NM_019101.2:c.115-145_115-143delinsCTT (APOM)	NP_061974.2:n.115-145_115-143delinsCTT
NR_045828.1:n.143-145_143-143delinsCTT (APOM)
XM_006715150.2:c.12-145_12-143delinsCTT (APOM)	XP_006715213.1:n.12-145_12-143delinsCTT
XM_011514895.1:c.-14+3992_-14+3994delinsAAG (BAG6)	XP_011513197.1:n.-14+3992_-14+3994delinsAAG
XM_006715150.3:c.12-145_12-143delinsCTT (APOM)	XP_006715213.1:n.12-145_12-143delinsCTT
XM_017011279.2:c.-14+3992_-14+3994delinsAAG (BAG6)	XP_016866768.1:n.-14+3992_-14+3994delinsAAG
XM_024446545.1:c.-14+1435_-14+1437delinsAAG (BAG6)	XP_024302313.1:n.-14+1435_-14+1437delinsAAG
NM_019101.3:c.115-145_115-143delinsCTT (APOM) MANE Select	NP_061974.2:n.115-145_115-143delinsCTT
NM_001256169.2:c.-102-145_-102-143delinsCTT (APOM)	NP_001243098.1:n.-102-145_-102-143delinsCTT
NR_045828.2:n.149-145_149-143delinsCTT (APOM)