Canonical Allele Identifier: CA1619250833

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657697_31657700delinsCCTT , CM000668.2:g.31657697_31657700delinsCCTT	GRCh38
NC_000006.11:g.31625474_31625477delinsCCTT , CM000668.1:g.31625474_31625477delinsCCTT	GRCh37
NC_000006.10:g.31733453_31733456delinsCCTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.515_518delinsCCTT (APOM) MANE Select	ENSP00000365081.3:p.Ala172=
ENST00000375916.3:c.515_518delinsCCTT (APOM)	ENSP00000365081.3:p.Ala172=
ENST00000375918.6:c.299_302delinsCCTT (APOM)	ENSP00000365083.2:p.Ala100=
ENST00000375920.8:c.299_302delinsCCTT (APOM)	ENSP00000365085.4:p.Ala100=
NM_001256169.1:c.299_302delinsCCTT (APOM)	NP_001243098.1:p.Ala100=
NM_019101.2:c.515_518delinsCCTT (APOM)	NP_061974.2:p.Ala172=
NR_045828.1:n.550_553delinsCCTT (APOM)
XM_006715150.2:c.419_422delinsCCTT (APOM)	XP_006715213.1:p.Ala140=
XM_011514895.1:c.-14+2621_-14+2624delinsAAGG (BAG6)	XP_011513197.1:n.-14+2621_-14+2624delinsAAGG
XM_006715150.3:c.419_422delinsCCTT (APOM)	XP_006715213.1:p.Ala140=
XM_017011279.2:c.-14+2621_-14+2624delinsAAGG (BAG6)	XP_016866768.1:n.-14+2621_-14+2624delinsAAGG
XM_024446545.1:c.-14+64_-14+67delinsAAGG (BAG6)	XP_024302313.1:n.-14+64_-14+67delinsAAGG
NM_019101.3:c.515_518delinsCCTT (APOM) MANE Select	NP_061974.2:p.Ala172=
NM_001256169.2:c.299_302delinsCCTT (APOM)	NP_001243098.1:p.Ala100=
NR_045828.2:n.556_559delinsCCTT (APOM)