Canonical Allele Identifier: CA1619250078

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31655873_31655874delinsGA , CM000668.2:g.31655873_31655874delinsGA	GRCh38
NC_000006.11:g.31623650_31623651delinsGA , CM000668.1:g.31623650_31623651delinsGA	GRCh37
NC_000006.10:g.31731629_31731630delinsGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.3:c.-94_-93delinsGA (APOM)	ENSP00000365081.3:n.-94_-93delinsGA
ENST00000375918.6:c.-102-599_-102-598delinsGA (APOM)	ENSP00000365083.2:n.-102-599_-102-598delinsGA
ENST00000375920.8:c.-102-599_-102-598delinsGA (APOM)	ENSP00000365085.4:n.-102-599_-102-598delinsGA
NM_001256169.1:c.-102-599_-102-598delinsGA (APOM)	NP_001243098.1:n.-102-599_-102-598delinsGA
NR_045828.1:n.143-599_143-598delinsGA (APOM)
XM_006715150.2:c.-197_-196delinsGA (APOM)	XP_006715213.1:n.-197_-196delinsGA
XM_011514895.1:c.-13-4098_-13-4097delinsTC (BAG6)	XP_011513197.1:n.-13-4098_-13-4097delinsTC
XM_017011279.2:c.-13-4098_-13-4097delinsTC (BAG6)	XP_016866768.1:n.-13-4098_-13-4097delinsTC
XM_024446545.1:c.-14+1890_-14+1891delinsTC (BAG6)	XP_024302313.1:n.-14+1890_-14+1891delinsTC
NM_001256169.2:c.-102-599_-102-598delinsGA (APOM)	NP_001243098.1:n.-102-599_-102-598delinsGA
NR_045828.2:n.149-599_149-598delinsGA (APOM)