Canonical Allele Identifier: CA2677982499

Gene: APOM BAG6

Linked Data

• gnomAD v4: 6-31655935-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31655935C>A , CM000668.2:g.31655935C>A	GRCh38
NC_000006.11:g.31623712C>A , CM000668.1:g.31623712C>A	GRCh37
NC_000006.10:g.31731691C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.-32C>A (APOM) MANE Select	ENSP00000365081.3:n.-32C>A
ENST00000375916.3:c.-32C>A (APOM)	ENSP00000365081.3:n.-32C>A
ENST00000375918.6:c.-102-537C>A (APOM)	ENSP00000365083.2:n.-102-537C>A
ENST00000375920.8:c.-102-537C>A (APOM)	ENSP00000365085.4:n.-102-537C>A
NM_001256169.1:c.-102-537C>A (APOM)	NP_001243098.1:n.-102-537C>A
NM_019101.2:c.-32C>A (APOM)	NP_061974.2:n.-32C>A
NR_045828.1:n.143-537C>A (APOM)
XM_006715150.2:c.-135C>A (APOM)	XP_006715213.1:n.-135C>A
XM_011514895.1:c.-13-4159G>T (BAG6)	XP_011513197.1:n.-13-4159G>T
XM_006715150.3:c.-135C>A (APOM)	XP_006715213.1:n.-135C>A
XM_017011279.2:c.-13-4159G>T (BAG6)	XP_016866768.1:n.-13-4159G>T
XM_024446545.1:c.-14+1829G>T (BAG6)	XP_024302313.1:n.-14+1829G>T
NM_019101.3:c.-32C>A (APOM) MANE Select	NP_061974.2:n.-32C>A
NM_001256169.2:c.-102-537C>A (APOM)	NP_001243098.1:n.-102-537C>A
NR_045828.2:n.149-537C>A (APOM)