Canonical Allele Identifier: CA2578566659

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31655916G>T , CM000668.2:g.31655916G>T	GRCh38
NC_000006.11:g.31623693G>T , CM000668.1:g.31623693G>T	GRCh37
NC_000006.10:g.31731672G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.-51G>T (APOM) MANE Select	ENSP00000365081.3:n.-51G>T
ENST00000375916.3:c.-51G>T (APOM)	ENSP00000365081.3:n.-51G>T
ENST00000375918.6:c.-102-556G>T (APOM)	ENSP00000365083.2:n.-102-556G>T
ENST00000375920.8:c.-102-556G>T (APOM)	ENSP00000365085.4:n.-102-556G>T
NM_001256169.1:c.-102-556G>T (APOM)	NP_001243098.1:n.-102-556G>T
NM_019101.2:c.-51G>T (APOM)	NP_061974.2:n.-51G>T
NR_045828.1:n.143-556G>T (APOM)
XM_006715150.2:c.-154G>T (APOM)	XP_006715213.1:n.-154G>T
XM_011514895.1:c.-13-4140C>A (BAG6)	XP_011513197.1:n.-13-4140C>A
XM_017011279.2:c.-13-4140C>A (BAG6)	XP_016866768.1:n.-13-4140C>A
XM_024446545.1:c.-14+1848C>A (BAG6)	XP_024302313.1:n.-14+1848C>A
NM_019101.3:c.-51G>T (APOM) MANE Select	NP_061974.2:n.-51G>T
NM_001256169.2:c.-102-556G>T (APOM)	NP_001243098.1:n.-102-556G>T
NR_045828.2:n.149-556G>T (APOM)