Canonical Allele Identifier: CA566364045

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1369107004
• gnomAD v2: 6-31624984-CCACCACCACCTCTGCAGGAAAG-C
• gnomAD v3: 6-31657207-CCACCACCACCTCTGCAGGAAAG-C
• gnomAD v4: 6-31657207-CCACCACCACCTCTGCAGGAAAG-C
• MyVariant Identifiers: chr6:g.31624985_31625006del (hg19) ; chr6:g.31657208_31657229del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657208_31657229del , CM000668.2:g.31657208_31657229del	GRCh38
NC_000006.11:g.31624985_31625006del , CM000668.1:g.31624985_31625006del	GRCh37
NC_000006.10:g.31732964_31732985del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.270-17_274del (APOM)
ENST00000375916.3:c.270-17_274del (APOM)
ENST00000375918.6:c.54-17_58del (APOM)
ENST00000375920.8:c.54-17_58del (APOM)
NM_001256169.1:c.54-17_58del (APOM)
NM_019101.2:c.270-17_274del (APOM)
NR_045828.1:n.305-17_309del (APOM)
XM_006715150.2:c.174-17_178del (APOM)
XM_011514895.1:c.-14+3092_-14+3113del (BAG6)	XP_011513197.1:n.-14+3092_-14+3113del
XM_006715150.3:c.174-17_178del (APOM)
XM_017011279.2:c.-14+3092_-14+3113del (BAG6)	XP_016866768.1:n.-14+3092_-14+3113del
XM_024446545.1:c.-14+535_-14+556del (BAG6)	XP_024302313.1:n.-14+535_-14+556del
NM_019101.3:c.270-17_274del (APOM)
NM_001256169.2:c.54-17_58del (APOM)
NR_045828.2:n.311-17_315del (APOM)