Canonical Allele Identifier: CA566364063

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1314928940
• gnomAD v2: 6-31625011-GCT-G
• gnomAD v4: 6-31657234-GCT-G
• MyVariant Identifiers: chr6:g.31625012_31625013del (hg19) ; chr6:g.31657235_31657236del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657237_31657238del , CM000668.2:g.31657237_31657238del	GRCh38
NC_000006.11:g.31625014_31625015del , CM000668.1:g.31625014_31625015del	GRCh37
NC_000006.10:g.31732993_31732994del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.282_283del (APOM) MANE Select	ENSP00000365081.3:p.Val96AlafsTer10
ENST00000375916.3:c.282_283del (APOM)	ENSP00000365081.3:p.Val96AlafsTer10
ENST00000375918.6:c.66_67del (APOM)	ENSP00000365083.2:p.Val24AlafsTer10
ENST00000375920.8:c.66_67del (APOM)	ENSP00000365085.4:p.Val24AlafsTer10
NM_001256169.1:c.66_67del (APOM)	NP_001243098.1:p.Val24AlafsTer10
NM_019101.2:c.282_283del (APOM)	NP_061974.2:p.Val96AlafsTer10
NR_045828.1:n.317_318del (APOM)
XM_006715150.2:c.186_187del (APOM)	XP_006715213.1:p.Val64AlafsTer10
XM_011514895.1:c.-14+3085_-14+3086del (BAG6)	XP_011513197.1:n.-14+3085_-14+3086del
XM_006715150.3:c.186_187del (APOM)	XP_006715213.1:p.Val64AlafsTer10
XM_017011279.2:c.-14+3085_-14+3086del (BAG6)	XP_016866768.1:n.-14+3085_-14+3086del
XM_024446545.1:c.-14+528_-14+529del (BAG6)	XP_024302313.1:n.-14+528_-14+529del
NM_019101.3:c.282_283del (APOM) MANE Select	NP_061974.2:p.Val96AlafsTer10
NM_001256169.2:c.66_67del (APOM)	NP_001243098.1:p.Val24AlafsTer10
NR_045828.2:n.323_324del (APOM)