Canonical Allele Identifier: CA1619251004

Linked Data

dbSNP Id: rs1800345209

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31658158del , CM000668.2:g.31658158del GRCh38
NC_000006.11:g.31625935del , CM000668.1:g.31625935del GRCh37
NC_000006.10:g.31733914del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.*69del (APOM) MANE Select ENSP00000365081.3:n.*69del
ENST00000375916.3:c.*69del (APOM) ENSP00000365081.3:n.*69del
ENST00000375920.8:c.*69del (APOM) ENSP00000365085.4:n.*69del
NM_001256169.1:c.*69del (APOM) NP_001243098.1:n.*69del
NM_019101.2:c.*69del (APOM) NP_061974.2:n.*69del
NR_045828.1:n.671del (APOM)
XM_006715150.2:c.*69del (APOM) XP_006715213.1:n.*69del
XM_011514895.1:c.-14+2163del (BAG6) XP_011513197.1:n.-14+2163del
XM_006715150.3:c.*69del (APOM) XP_006715213.1:n.*69del
XM_017011279.2:c.-14+2163del (BAG6) XP_016866768.1:n.-14+2163del
NM_019101.3:c.*69del (APOM) MANE Select NP_061974.2:n.*69del
NM_001256169.2:c.*69del (APOM) NP_001243098.1:n.*69del
NR_045828.2:n.677del (APOM)