Canonical Allele Identifier: CA363427477

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1583541417
• COSMIC: COSM5014582 ; COSM5014583
• MyVariant Identifiers: chr6:g.31625169T>C (hg19) ; chr6:g.31657392T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657392T>C , CM000668.2:g.31657392T>C	GRCh38
NC_000006.11:g.31625169T>C , CM000668.1:g.31625169T>C	GRCh37
NC_000006.10:g.31733148T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.356T>C (APOM) MANE Select	ENSP00000365081.3:p.Met119Thr
ENST00000375916.3:c.356T>C (APOM)	ENSP00000365081.3:p.Met119Thr
ENST00000375918.6:c.140T>C (APOM)	ENSP00000365083.2:p.Met47Thr
ENST00000375920.8:c.140T>C (APOM)	ENSP00000365085.4:p.Met47Thr
NM_001256169.1:c.140T>C (APOM)	NP_001243098.1:p.Met47Thr
NM_019101.2:c.356T>C (APOM)	NP_061974.2:p.Met119Thr
NR_045828.1:n.391T>C (APOM)
XM_006715150.2:c.260T>C (APOM)	XP_006715213.1:p.Met87Thr
XM_011514895.1:c.-14+2929A>G (BAG6)	XP_011513197.1:n.-14+2929A>G
XM_006715150.3:c.260T>C (APOM)	XP_006715213.1:p.Met87Thr
XM_017011279.2:c.-14+2929A>G (BAG6)	XP_016866768.1:n.-14+2929A>G
XM_024446545.1:c.-14+372A>G (BAG6)	XP_024302313.1:n.-14+372A>G
NM_019101.3:c.356T>C (APOM) MANE Select	NP_061974.2:p.Met119Thr
NM_001256169.2:c.140T>C (APOM)	NP_001243098.1:p.Met47Thr
NR_045828.2:n.397T>C (APOM)