Canonical Allele Identifier: CA1619250079

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1799985712

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31655875del , CM000668.2:g.31655875del	GRCh38
NC_000006.11:g.31623652del , CM000668.1:g.31623652del	GRCh37
NC_000006.10:g.31731631del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.3:c.-92del (APOM)	ENSP00000365081.3:n.-92del
ENST00000375918.6:c.-102-597del (APOM)	ENSP00000365083.2:n.-102-597del
ENST00000375920.8:c.-102-597del (APOM)	ENSP00000365085.4:n.-102-597del
NM_001256169.1:c.-102-597del (APOM)	NP_001243098.1:n.-102-597del
NR_045828.1:n.143-597del (APOM)
XM_006715150.2:c.-195del (APOM)	XP_006715213.1:n.-195del
XM_011514895.1:c.-13-4098del (BAG6)	XP_011513197.1:n.-13-4098del
XM_017011279.2:c.-13-4098del (BAG6)	XP_016866768.1:n.-13-4098del
XM_024446545.1:c.-14+1890del (BAG6)	XP_024302313.1:n.-14+1890del
NM_001256169.2:c.-102-597del (APOM)	NP_001243098.1:n.-102-597del
NR_045828.2:n.149-597del (APOM)