Canonical Allele Identifier: CA1619250739

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1800237455

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657477_31657478del , CM000668.2:g.31657477_31657478del	GRCh38
NC_000006.11:g.31625254_31625255del , CM000668.1:g.31625254_31625255del	GRCh37
NC_000006.10:g.31733233_31733234del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.441_442del (APOM) MANE Select	ENSP00000365081.3:p.Tyr147Ter
ENST00000375916.3:c.441_442del (APOM)	ENSP00000365081.3:p.Tyr147Ter
ENST00000375918.6:c.225_226del (APOM)	ENSP00000365083.2:p.Tyr75Ter
ENST00000375920.8:c.225_226del (APOM)	ENSP00000365085.4:p.Tyr75Ter
NM_001256169.1:c.225_226del (APOM)	NP_001243098.1:p.Tyr75Ter
NM_019101.2:c.441_442del (APOM)	NP_061974.2:p.Tyr147Ter
NR_045828.1:n.476_477del (APOM)
XM_006715150.2:c.345_346del (APOM)	XP_006715213.1:p.Tyr115Ter
XM_011514895.1:c.-14+2844_-14+2845del (BAG6)	XP_011513197.1:n.-14+2844_-14+2845del
XM_006715150.3:c.345_346del (APOM)	XP_006715213.1:p.Tyr115Ter
XM_017011279.2:c.-14+2844_-14+2845del (BAG6)	XP_016866768.1:n.-14+2844_-14+2845del
XM_024446545.1:c.-14+287_-14+288del (BAG6)	XP_024302313.1:n.-14+287_-14+288del
NM_019101.3:c.441_442del (APOM) MANE Select	NP_061974.2:p.Tyr147Ter
NM_001256169.2:c.225_226del (APOM)	NP_001243098.1:p.Tyr75Ter
NR_045828.2:n.482_483del (APOM)