Canonical Allele Identifier: CA650848206

Gene: APOM BAG6

Linked Data

• COSMIC: COSN20075687

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31658098T>C , CM000668.2:g.31658098T>C	GRCh38
NC_000006.11:g.31625875T>C , CM000668.1:g.31625875T>C	GRCh37
NC_000006.10:g.31733854T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.*9T>C (APOM) MANE Select	ENSP00000365081.3:n.*9T>C
ENST00000375916.3:c.*9T>C (APOM)	ENSP00000365081.3:n.*9T>C
ENST00000375920.8:c.*9T>C (APOM)	ENSP00000365085.4:n.*9T>C
NM_001256169.1:c.*9T>C (APOM)	NP_001243098.1:n.*9T>C
NM_019101.2:c.*9T>C (APOM)	NP_061974.2:n.*9T>C
NR_045828.1:n.611T>C (APOM)
XM_006715150.2:c.*9T>C (APOM)	XP_006715213.1:n.*9T>C
XM_011514895.1:c.-14+2223A>G (BAG6)	XP_011513197.1:n.-14+2223A>G
XM_006715150.3:c.*9T>C (APOM)	XP_006715213.1:n.*9T>C
XM_017011279.2:c.-14+2223A>G (BAG6)	XP_016866768.1:n.-14+2223A>G
NM_019101.3:c.*9T>C (APOM) MANE Select	NP_061974.2:n.*9T>C
NM_001256169.2:c.*9T>C (APOM)	NP_001243098.1:n.*9T>C
NR_045828.2:n.617T>C (APOM)