Canonical Allele Identifier: CA1619250960

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1800328646

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31658034dup , CM000668.2:g.31658034dup	GRCh38
NC_000006.11:g.31625811dup , CM000668.1:g.31625811dup	GRCh37
NC_000006.10:g.31733790dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.542-30dup (APOM) MANE Select	ENSP00000365081.3:n.542-30dup
ENST00000375916.3:c.542-30dup (APOM)	ENSP00000365081.3:n.542-30dup
ENST00000375918.6:c.*246dup (APOM)	ENSP00000365083.2:n.*246dup
ENST00000375920.8:c.326-30dup (APOM)	ENSP00000365085.4:n.326-30dup
NM_001256169.1:c.326-30dup (APOM)	NP_001243098.1:n.326-30dup
NM_019101.2:c.542-30dup (APOM)	NP_061974.2:n.542-30dup
NR_045828.1:n.577-30dup (APOM)
XM_006715150.2:c.446-30dup (APOM)	XP_006715213.1:n.446-30dup
XM_011514895.1:c.-14+2287dup (BAG6)	XP_011513197.1:n.-14+2287dup
XM_006715150.3:c.446-30dup (APOM)	XP_006715213.1:n.446-30dup
XM_017011279.2:c.-14+2287dup (BAG6)	XP_016866768.1:n.-14+2287dup
NM_019101.3:c.542-30dup (APOM) MANE Select	NP_061974.2:n.542-30dup
NM_001256169.2:c.326-30dup (APOM)	NP_001243098.1:n.326-30dup
NR_045828.2:n.583-30dup (APOM)