Canonical Allele Identifier: CA1619250599

Linked Data

dbSNP Id: rs1800180198

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657159_31657162del , CM000668.2:g.31657159_31657162del GRCh38
NC_000006.11:g.31624936_31624939del , CM000668.1:g.31624936_31624939del GRCh37
NC_000006.10:g.31732915_31732918del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.270-66_270-63del (APOM) MANE Select ENSP00000365081.3:n.270-66_270-63del
ENST00000375916.3:c.270-66_270-63del (APOM) ENSP00000365081.3:n.270-66_270-63del
ENST00000375918.6:c.54-66_54-63del (APOM) ENSP00000365083.2:n.54-66_54-63del
ENST00000375920.8:c.54-66_54-63del (APOM) ENSP00000365085.4:n.54-66_54-63del
NM_001256169.1:c.54-66_54-63del (APOM) NP_001243098.1:n.54-66_54-63del
NM_019101.2:c.270-66_270-63del (APOM) NP_061974.2:n.270-66_270-63del
NR_045828.1:n.305-66_305-63del (APOM)
XM_006715150.2:c.174-66_174-63del (APOM) XP_006715213.1:n.174-66_174-63del
XM_011514895.1:c.-14+3161_-14+3164del (BAG6) XP_011513197.1:n.-14+3161_-14+3164del
XM_006715150.3:c.174-66_174-63del (APOM) XP_006715213.1:n.174-66_174-63del
XM_017011279.2:c.-14+3161_-14+3164del (BAG6) XP_016866768.1:n.-14+3161_-14+3164del
XM_024446545.1:c.-14+604_-14+607del (BAG6) XP_024302313.1:n.-14+604_-14+607del
NM_019101.3:c.270-66_270-63del (APOM) MANE Select NP_061974.2:n.270-66_270-63del
NM_001256169.2:c.54-66_54-63del (APOM) NP_001243098.1:n.54-66_54-63del
NR_045828.2:n.311-66_311-63del (APOM)