Canonical Allele Identifier: CA136880297

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs933829549
• gnomAD v3: 6-31656721-C-CT
• gnomAD v4: 6-31656721-C-CT
• MyVariant Identifiers: chr6:g.31624498_31624499insT (hg19) ; chr6:g.31656721_31656722insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31656722dup , CM000668.2:g.31656722dup	GRCh38
NC_000006.11:g.31624499dup , CM000668.1:g.31624499dup	GRCh37
NC_000006.10:g.31732478dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.269+96dup (APOM) MANE Select	ENSP00000365081.3:n.269+96dup
ENST00000375916.3:c.269+96dup (APOM)	ENSP00000365081.3:n.269+96dup
ENST00000375918.6:c.53+96dup (APOM)	ENSP00000365083.2:n.53+96dup
ENST00000375920.8:c.53+96dup (APOM)	ENSP00000365085.4:n.53+96dup
NM_001256169.1:c.53+96dup (APOM)	NP_001243098.1:n.53+96dup
NM_019101.2:c.269+96dup (APOM)	NP_061974.2:n.269+96dup
NR_045828.1:n.304+89dup (APOM)
XM_006715150.2:c.173+89dup (APOM)	XP_006715213.1:n.173+89dup
XM_011514895.1:c.-14+3599dup (BAG6)	XP_011513197.1:n.-14+3599dup
XM_006715150.3:c.173+89dup (APOM)	XP_006715213.1:n.173+89dup
XM_017011279.2:c.-14+3599dup (BAG6)	XP_016866768.1:n.-14+3599dup
XM_024446545.1:c.-14+1042dup (BAG6)	XP_024302313.1:n.-14+1042dup
NM_019101.3:c.269+96dup (APOM) MANE Select	NP_061974.2:n.269+96dup
NM_001256169.2:c.53+96dup (APOM)	NP_001243098.1:n.53+96dup
NR_045828.2:n.310+89dup (APOM)