Canonical Allele Identifier: CA566364350

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1404226582
• gnomAD v2: 6-31625814-CCTT-C
• gnomAD v4: 6-31658037-CCTT-C
• MyVariant Identifiers: chr6:g.31625815_31625817del (hg19) ; chr6:g.31658038_31658040del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31658041_31658043del , CM000668.2:g.31658041_31658043del	GRCh38
NC_000006.11:g.31625818_31625820del , CM000668.1:g.31625818_31625820del	GRCh37
NC_000006.10:g.31733797_31733799del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.542-23_542-21del (APOM) MANE Select	ENSP00000365081.3:n.542-23_542-21del
ENST00000375916.3:c.542-23_542-21del (APOM)	ENSP00000365081.3:n.542-23_542-21del
ENST00000375918.6:c.*253_*255del (APOM)	ENSP00000365083.2:n.*253_*255del
ENST00000375920.8:c.326-23_326-21del (APOM)	ENSP00000365085.4:n.326-23_326-21del
NM_001256169.1:c.326-23_326-21del (APOM)	NP_001243098.1:n.326-23_326-21del
NM_019101.2:c.542-23_542-21del (APOM)	NP_061974.2:n.542-23_542-21del
NR_045828.1:n.577-23_577-21del (APOM)
XM_006715150.2:c.446-23_446-21del (APOM)	XP_006715213.1:n.446-23_446-21del
XM_011514895.1:c.-14+2281_-14+2283del (BAG6)	XP_011513197.1:n.-14+2281_-14+2283del
XM_006715150.3:c.446-23_446-21del (APOM)	XP_006715213.1:n.446-23_446-21del
XM_017011279.2:c.-14+2281_-14+2283del (BAG6)	XP_016866768.1:n.-14+2281_-14+2283del
NM_019101.3:c.542-23_542-21del (APOM) MANE Select	NP_061974.2:n.542-23_542-21del
NM_001256169.2:c.326-23_326-21del (APOM)	NP_001243098.1:n.326-23_326-21del
NR_045828.2:n.583-23_583-21del (APOM)