Canonical Allele Identifier: CA363429677

Gene: APOM BAG6

Linked Data

• COSMIC: COSM1311995
• MyVariant Identifiers: chr6:g.31625244T>G (hg19) ; chr6:g.31657467T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657467T>G , CM000668.2:g.31657467T>G	GRCh38
NC_000006.11:g.31625244T>G , CM000668.1:g.31625244T>G	GRCh37
NC_000006.10:g.31733223T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.431T>G (APOM) MANE Select	ENSP00000365081.3:p.Phe144Cys
ENST00000375916.3:c.431T>G (APOM)	ENSP00000365081.3:p.Phe144Cys
ENST00000375918.6:c.215T>G (APOM)	ENSP00000365083.2:p.Phe72Cys
ENST00000375920.8:c.215T>G (APOM)	ENSP00000365085.4:p.Phe72Cys
NM_001256169.1:c.215T>G (APOM)	NP_001243098.1:p.Phe72Cys
NM_019101.2:c.431T>G (APOM)	NP_061974.2:p.Phe144Cys
NR_045828.1:n.466T>G (APOM)
XM_006715150.2:c.335T>G (APOM)	XP_006715213.1:p.Phe112Cys
XM_011514895.1:c.-14+2854A>C (BAG6)	XP_011513197.1:n.-14+2854A>C
XM_006715150.3:c.335T>G (APOM)	XP_006715213.1:p.Phe112Cys
XM_017011279.2:c.-14+2854A>C (BAG6)	XP_016866768.1:n.-14+2854A>C
XM_024446545.1:c.-14+297A>C (BAG6)	XP_024302313.1:n.-14+297A>C
NM_019101.3:c.431T>G (APOM) MANE Select	NP_061974.2:p.Phe144Cys
NM_001256169.2:c.215T>G (APOM)	NP_001243098.1:p.Phe72Cys
NR_045828.2:n.472T>G (APOM)