Canonical Allele Identifier: CA2711458011

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs2151145127

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657153_31657154insG , CM000668.2:g.31657153_31657154insG	GRCh38
NC_000006.11:g.31624930_31624931insG , CM000668.1:g.31624930_31624931insG	GRCh37
NC_000006.10:g.31732909_31732910insG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.270-72_270-71insG (APOM) MANE Select	ENSP00000365081.3:n.270-72_270-71insG
ENST00000375916.3:c.270-72_270-71insG (APOM)	ENSP00000365081.3:n.270-72_270-71insG
ENST00000375918.6:c.54-72_54-71insG (APOM)	ENSP00000365083.2:n.54-72_54-71insG
ENST00000375920.8:c.54-72_54-71insG (APOM)	ENSP00000365085.4:n.54-72_54-71insG
NM_001256169.1:c.54-72_54-71insG (APOM)	NP_001243098.1:n.54-72_54-71insG
NM_019101.2:c.270-72_270-71insG (APOM)	NP_061974.2:n.270-72_270-71insG
NR_045828.1:n.305-72_305-71insG (APOM)
XM_006715150.2:c.174-72_174-71insG (APOM)	XP_006715213.1:n.174-72_174-71insG
XM_011514895.1:c.-14+3167_-14+3168insC (BAG6)	XP_011513197.1:n.-14+3167_-14+3168insC
XM_006715150.3:c.174-72_174-71insG (APOM)	XP_006715213.1:n.174-72_174-71insG
XM_017011279.2:c.-14+3167_-14+3168insC (BAG6)	XP_016866768.1:n.-14+3167_-14+3168insC
XM_024446545.1:c.-14+610_-14+611insC (BAG6)	XP_024302313.1:n.-14+610_-14+611insC
NM_019101.3:c.270-72_270-71insG (APOM) MANE Select	NP_061974.2:n.270-72_270-71insG
NM_001256169.2:c.54-72_54-71insG (APOM)	NP_001243098.1:n.54-72_54-71insG
NR_045828.2:n.311-72_311-71insG (APOM)