Canonical Allele Identifier: CA1087477113

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1800143851
• gnomAD v3: 6-31656953-TGGCTAACACA-T
• gnomAD v4: 6-31656953-TGGCTAACACA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31656955_31656964del , CM000668.2:g.31656955_31656964del	GRCh38
NC_000006.11:g.31624732_31624741del , CM000668.1:g.31624732_31624741del	GRCh37
NC_000006.10:g.31732711_31732720del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.270-270_270-261del (APOM) MANE Select	ENSP00000365081.3:n.270-270_270-261del
ENST00000375916.3:c.270-270_270-261del (APOM)	ENSP00000365081.3:n.270-270_270-261del
ENST00000375918.6:c.54-270_54-261del (APOM)	ENSP00000365083.2:n.54-270_54-261del
ENST00000375920.8:c.54-270_54-261del (APOM)	ENSP00000365085.4:n.54-270_54-261del
NM_001256169.1:c.54-270_54-261del (APOM)	NP_001243098.1:n.54-270_54-261del
NM_019101.2:c.270-270_270-261del (APOM)	NP_061974.2:n.270-270_270-261del
NR_045828.1:n.305-270_305-261del (APOM)
XM_006715150.2:c.174-270_174-261del (APOM)	XP_006715213.1:n.174-270_174-261del
XM_011514895.1:c.-14+3358_-14+3367del (BAG6)	XP_011513197.1:n.-14+3358_-14+3367del
XM_006715150.3:c.174-270_174-261del (APOM)	XP_006715213.1:n.174-270_174-261del
XM_017011279.2:c.-14+3358_-14+3367del (BAG6)	XP_016866768.1:n.-14+3358_-14+3367del
XM_024446545.1:c.-14+801_-14+810del (BAG6)	XP_024302313.1:n.-14+801_-14+810del
NM_019101.3:c.270-270_270-261del (APOM) MANE Select	NP_061974.2:n.270-270_270-261del
NM_001256169.2:c.54-270_54-261del (APOM)	NP_001243098.1:n.54-270_54-261del
NR_045828.2:n.311-270_311-261del (APOM)