Canonical Allele Identifier: CA2677983246

Gene: APOM BAG6

Linked Data

• gnomAD v4: 6-31656717-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31656718dup , CM000668.2:g.31656718dup	GRCh38
NC_000006.11:g.31624495dup , CM000668.1:g.31624495dup	GRCh37
NC_000006.10:g.31732474dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.269+92dup (APOM) MANE Select	ENSP00000365081.3:n.269+92dup
ENST00000375916.3:c.269+92dup (APOM)	ENSP00000365081.3:n.269+92dup
ENST00000375918.6:c.53+92dup (APOM)	ENSP00000365083.2:n.53+92dup
ENST00000375920.8:c.53+92dup (APOM)	ENSP00000365085.4:n.53+92dup
NM_001256169.1:c.53+92dup (APOM)	NP_001243098.1:n.53+92dup
NM_019101.2:c.269+92dup (APOM)	NP_061974.2:n.269+92dup
NR_045828.1:n.304+85dup (APOM)
XM_006715150.2:c.173+85dup (APOM)	XP_006715213.1:n.173+85dup
XM_011514895.1:c.-14+3603dup (BAG6)	XP_011513197.1:n.-14+3603dup
XM_006715150.3:c.173+85dup (APOM)	XP_006715213.1:n.173+85dup
XM_017011279.2:c.-14+3603dup (BAG6)	XP_016866768.1:n.-14+3603dup
XM_024446545.1:c.-14+1046dup (BAG6)	XP_024302313.1:n.-14+1046dup
NM_019101.3:c.269+92dup (APOM) MANE Select	NP_061974.2:n.269+92dup
NM_001256169.2:c.53+92dup (APOM)	NP_001243098.1:n.53+92dup
NR_045828.2:n.310+85dup (APOM)