Canonical Allele Identifier: CA1619250774

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657558_31657562delinsACCCT , CM000668.2:g.31657558_31657562delinsACCCT	GRCh38
NC_000006.11:g.31625335_31625339delinsACCCT , CM000668.1:g.31625335_31625339delinsACCCT	GRCh37
NC_000006.10:g.31733314_31733318delinsACCCT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.443-67_443-63delinsACCCT (APOM) MANE Select	ENSP00000365081.3:n.443-67_443-63delinsAC...
ENST00000375916.3:c.443-67_443-63delinsACCCT (APOM)	ENSP00000365081.3:n.443-67_443-63delinsAC...
ENST00000375918.6:c.227-67_227-63delinsACCCT (APOM)	ENSP00000365083.2:n.227-67_227-63delinsAC...
ENST00000375920.8:c.227-67_227-63delinsACCCT (APOM)	ENSP00000365085.4:n.227-67_227-63delinsAC...
NM_001256169.1:c.227-67_227-63delinsACCCT (APOM)	NP_001243098.1:n.227-67_227-63delinsACCCT...
NM_019101.2:c.443-67_443-63delinsACCCT (APOM)	NP_061974.2:n.443-67_443-63delinsACCCT
NR_045828.1:n.478-67_478-63delinsACCCT (APOM)
XM_006715150.2:c.347-67_347-63delinsACCCT (APOM)	XP_006715213.1:n.347-67_347-63delinsACCCT...
XM_011514895.1:c.-14+2759_-14+2763delinsAGGGT (BAG6)	XP_011513197.1:n.-14+2759_-14+2763delinsA...
XM_006715150.3:c.347-67_347-63delinsACCCT (APOM)	XP_006715213.1:n.347-67_347-63delinsACCCT...
XM_017011279.2:c.-14+2759_-14+2763delinsAGGGT (BAG6)	XP_016866768.1:n.-14+2759_-14+2763delinsA...
XM_024446545.1:c.-14+202_-14+206delinsAGGGT (BAG6)	XP_024302313.1:n.-14+202_-14+206delinsAGG...
NM_019101.3:c.443-67_443-63delinsACCCT (APOM) MANE Select	NP_061974.2:n.443-67_443-63delinsACCCT
NM_001256169.2:c.227-67_227-63delinsACCCT (APOM)	NP_001243098.1:n.227-67_227-63delinsACCCT...
NR_045828.2:n.484-67_484-63delinsACCCT (APOM)