Canonical Allele Identifier: CA1619250760

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657522_31657523delinsGA , CM000668.2:g.31657522_31657523delinsGA	GRCh38
NC_000006.11:g.31625299_31625300delinsGA , CM000668.1:g.31625299_31625300delinsGA	GRCh37
NC_000006.10:g.31733278_31733279delinsGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.442+44_442+45delinsGA (APOM) MANE Select	ENSP00000365081.3:n.442+44_442+45delinsGA
ENST00000375916.3:c.442+44_442+45delinsGA (APOM)	ENSP00000365081.3:n.442+44_442+45delinsGA
ENST00000375918.6:c.226+44_226+45delinsGA (APOM)	ENSP00000365083.2:n.226+44_226+45delinsGA
ENST00000375920.8:c.226+44_226+45delinsGA (APOM)	ENSP00000365085.4:n.226+44_226+45delinsGA
NM_001256169.1:c.226+44_226+45delinsGA (APOM)	NP_001243098.1:n.226+44_226+45delinsGA
NM_019101.2:c.442+44_442+45delinsGA (APOM)	NP_061974.2:n.442+44_442+45delinsGA
NR_045828.1:n.477+44_477+45delinsGA (APOM)
XM_006715150.2:c.346+44_346+45delinsGA (APOM)	XP_006715213.1:n.346+44_346+45delinsGA
XM_011514895.1:c.-14+2798_-14+2799delinsTC (BAG6)	XP_011513197.1:n.-14+2798_-14+2799delinsTC
XM_006715150.3:c.346+44_346+45delinsGA (APOM)	XP_006715213.1:n.346+44_346+45delinsGA
XM_017011279.2:c.-14+2798_-14+2799delinsTC (BAG6)	XP_016866768.1:n.-14+2798_-14+2799delinsTC
XM_024446545.1:c.-14+241_-14+242delinsTC (BAG6)	XP_024302313.1:n.-14+241_-14+242delinsTC
NM_019101.3:c.442+44_442+45delinsGA (APOM) MANE Select	NP_061974.2:n.442+44_442+45delinsGA
NM_001256169.2:c.226+44_226+45delinsGA (APOM)	NP_001243098.1:n.226+44_226+45delinsGA
NR_045828.2:n.483+44_483+45delinsGA (APOM)