Canonical Allele Identifier: CA2770506280

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31658139_31658141del , CM000668.2:g.31658139_31658141del	GRCh38
NC_000006.11:g.31625916_31625918del , CM000668.1:g.31625916_31625918del	GRCh37
NC_000006.10:g.31733895_31733897del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.*50_*52del (APOM) MANE Select	ENSP00000365081.3:n.*50_*52del
ENST00000375916.3:c.*50_*52del (APOM)	ENSP00000365081.3:n.*50_*52del
ENST00000375920.8:c.*50_*52del (APOM)	ENSP00000365085.4:n.*50_*52del
NM_001256169.1:c.*50_*52del (APOM)	NP_001243098.1:n.*50_*52del
NM_019101.2:c.*50_*52del (APOM)	NP_061974.2:n.*50_*52del
NR_045828.1:n.652_654del (APOM)
XM_006715150.2:c.*50_*52del (APOM)	XP_006715213.1:n.*50_*52del
XM_011514895.1:c.-14+2184_-14+2186del (BAG6)	XP_011513197.1:n.-14+2184_-14+2186del
XM_006715150.3:c.*50_*52del (APOM)	XP_006715213.1:n.*50_*52del
XM_017011279.2:c.-14+2184_-14+2186del (BAG6)	XP_016866768.1:n.-14+2184_-14+2186del
NM_019101.3:c.*50_*52del (APOM) MANE Select	NP_061974.2:n.*50_*52del
NM_001256169.2:c.*50_*52del (APOM)	NP_001243098.1:n.*50_*52del
NR_045828.2:n.658_660del (APOM)