Canonical Allele Identifier: CA2677983834

Gene: APOM BAG6

Linked Data

• gnomAD v4: 6-31657502-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657505del , CM000668.2:g.31657505del	GRCh38
NC_000006.11:g.31625282del , CM000668.1:g.31625282del	GRCh37
NC_000006.10:g.31733261del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.442+27del (APOM) MANE Select	ENSP00000365081.3:n.442+27del
ENST00000375916.3:c.442+27del (APOM)	ENSP00000365081.3:n.442+27del
ENST00000375918.6:c.226+27del (APOM)	ENSP00000365083.2:n.226+27del
ENST00000375920.8:c.226+27del (APOM)	ENSP00000365085.4:n.226+27del
NM_001256169.1:c.226+27del (APOM)	NP_001243098.1:n.226+27del
NM_019101.2:c.442+27del (APOM)	NP_061974.2:n.442+27del
NR_045828.1:n.477+27del (APOM)
XM_006715150.2:c.346+27del (APOM)	XP_006715213.1:n.346+27del
XM_011514895.1:c.-14+2818del (BAG6)	XP_011513197.1:n.-14+2818del
XM_006715150.3:c.346+27del (APOM)	XP_006715213.1:n.346+27del
XM_017011279.2:c.-14+2818del (BAG6)	XP_016866768.1:n.-14+2818del
XM_024446545.1:c.-14+261del (BAG6)	XP_024302313.1:n.-14+261del
NM_019101.3:c.442+27del (APOM) MANE Select	NP_061974.2:n.442+27del
NM_001256169.2:c.226+27del (APOM)	NP_001243098.1:n.226+27del
NR_045828.2:n.483+27del (APOM)