Canonical Allele Identifier: CA823895845

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1243761806
• gnomAD v3: 6-31657558-ACCCT-A
• gnomAD v4: 6-31657558-ACCCT-A
• MyVariant Identifiers: chr6:g.31625336_31625339del (hg19) ; chr6:g.31657559_31657562del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657562_31657565del , CM000668.2:g.31657562_31657565del	GRCh38
NC_000006.11:g.31625339_31625342del , CM000668.1:g.31625339_31625342del	GRCh37
NC_000006.10:g.31733318_31733321del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.443-63_443-60del (APOM) MANE Select	ENSP00000365081.3:n.443-63_443-60del
ENST00000375916.3:c.443-63_443-60del (APOM)	ENSP00000365081.3:n.443-63_443-60del
ENST00000375918.6:c.227-63_227-60del (APOM)	ENSP00000365083.2:n.227-63_227-60del
ENST00000375920.8:c.227-63_227-60del (APOM)	ENSP00000365085.4:n.227-63_227-60del
NM_001256169.1:c.227-63_227-60del (APOM)	NP_001243098.1:n.227-63_227-60del
NM_019101.2:c.443-63_443-60del (APOM)	NP_061974.2:n.443-63_443-60del
NR_045828.1:n.478-63_478-60del (APOM)
XM_006715150.2:c.347-63_347-60del (APOM)	XP_006715213.1:n.347-63_347-60del
XM_011514895.1:c.-14+2759_-14+2762del (BAG6)	XP_011513197.1:n.-14+2759_-14+2762del
XM_006715150.3:c.347-63_347-60del (APOM)	XP_006715213.1:n.347-63_347-60del
XM_017011279.2:c.-14+2759_-14+2762del (BAG6)	XP_016866768.1:n.-14+2759_-14+2762del
XM_024446545.1:c.-14+202_-14+205del (BAG6)	XP_024302313.1:n.-14+202_-14+205del
NM_019101.3:c.443-63_443-60del (APOM) MANE Select	NP_061974.2:n.443-63_443-60del
NM_001256169.2:c.227-63_227-60del (APOM)	NP_001243098.1:n.227-63_227-60del
NR_045828.2:n.484-63_484-60del (APOM)