Canonical Allele Identifier: CA2677983777

Gene: APOM BAG6

Linked Data

• gnomAD v4: 6-31657373-T-TTGACAGGCCGCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657379_31657391dup , CM000668.2:g.31657379_31657391dup	GRCh38
NC_000006.11:g.31625156_31625168dup , CM000668.1:g.31625156_31625168dup	GRCh37
NC_000006.10:g.31733135_31733147dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.344-1_355dup (APOM)
ENST00000375916.3:c.344-1_355dup (APOM)
ENST00000375918.6:c.128-1_139dup (APOM)
ENST00000375920.8:c.128-1_139dup (APOM)
NM_001256169.1:c.128-1_139dup (APOM)
NM_019101.2:c.344-1_355dup (APOM)
NR_045828.1:n.379-1_390dup (APOM)
XM_006715150.2:c.248-1_259dup (APOM)
XM_011514895.1:c.-14+2935_-14+2947dup (BAG6)	XP_011513197.1:n.-14+2935_-14+2947dup
XM_006715150.3:c.248-1_259dup (APOM)
XM_017011279.2:c.-14+2935_-14+2947dup (BAG6)	XP_016866768.1:n.-14+2935_-14+2947dup
XM_024446545.1:c.-14+378_-14+390dup (BAG6)	XP_024302313.1:n.-14+378_-14+390dup
NM_019101.3:c.344-1_355dup (APOM)
NM_001256169.2:c.128-1_139dup (APOM)
NR_045828.2:n.385-1_396dup (APOM)