Canonical Allele Identifier: CA1619249368

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31654038A= , CM000668.2:g.31654038A=	GRCh38
NC_000006.11:g.31621815A= , CM000668.1:g.31621815A=	GRCh37
NC_000006.10:g.31729794A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375918.6:c.-103+1487A= (APOM)	ENSP00000365083.2:n.-103+1487A=
ENST00000375920.8:c.-103+1487A= (APOM)	ENSP00000365085.4:n.-103+1487A=
NM_001256169.1:c.-103+1487A= (APOM)	NP_001243098.1:n.-103+1487A=
NR_045828.1:n.142+1487A= (APOM)
XM_011514895.1:c.-13-2262T= (BAG6)	XP_011513197.1:n.-13-2262T=
XM_017011279.2:c.-13-2262T= (BAG6)	XP_016866768.1:n.-13-2262T=
XM_024446545.1:c.-13-2262T= (BAG6)	XP_024302313.1:n.-13-2262T=
NM_001256169.2:c.-103+1487A= (APOM)	NP_001243098.1:n.-103+1487A=
NR_045828.2:n.148+1487A= (APOM)