Canonical Allele Identifier: CA2677983879

Gene: APOM BAG6

Linked Data

• gnomAD v4: 6-31657579-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657580del , CM000668.2:g.31657580del	GRCh38
NC_000006.11:g.31625357del , CM000668.1:g.31625357del	GRCh37
NC_000006.10:g.31733336del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.443-45del (APOM) MANE Select	ENSP00000365081.3:n.443-45del
ENST00000375916.3:c.443-45del (APOM)	ENSP00000365081.3:n.443-45del
ENST00000375918.6:c.227-45del (APOM)	ENSP00000365083.2:n.227-45del
ENST00000375920.8:c.227-45del (APOM)	ENSP00000365085.4:n.227-45del
NM_001256169.1:c.227-45del (APOM)	NP_001243098.1:n.227-45del
NM_019101.2:c.443-45del (APOM)	NP_061974.2:n.443-45del
NR_045828.1:n.478-45del (APOM)
XM_006715150.2:c.347-45del (APOM)	XP_006715213.1:n.347-45del
XM_011514895.1:c.-14+2741del (BAG6)	XP_011513197.1:n.-14+2741del
XM_006715150.3:c.347-45del (APOM)	XP_006715213.1:n.347-45del
XM_017011279.2:c.-14+2741del (BAG6)	XP_016866768.1:n.-14+2741del
XM_024446545.1:c.-14+184del (BAG6)	XP_024302313.1:n.-14+184del
NM_019101.3:c.443-45del (APOM) MANE Select	NP_061974.2:n.443-45del
NM_001256169.2:c.227-45del (APOM)	NP_001243098.1:n.227-45del
NR_045828.2:n.484-45del (APOM)