Canonical Allele Identifier: CA1087477192

Linked Data

dbSNP Id: rs1800170413

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657132_31657135del , CM000668.2:g.31657132_31657135del GRCh38
NC_000006.11:g.31624909_31624912del , CM000668.1:g.31624909_31624912del GRCh37
NC_000006.10:g.31732888_31732891del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.270-93_270-90del (APOM) MANE Select ENSP00000365081.3:n.270-93_270-90del
ENST00000375916.3:c.270-93_270-90del (APOM) ENSP00000365081.3:n.270-93_270-90del
ENST00000375918.6:c.54-93_54-90del (APOM) ENSP00000365083.2:n.54-93_54-90del
ENST00000375920.8:c.54-93_54-90del (APOM) ENSP00000365085.4:n.54-93_54-90del
NM_001256169.1:c.54-93_54-90del (APOM) NP_001243098.1:n.54-93_54-90del
NM_019101.2:c.270-93_270-90del (APOM) NP_061974.2:n.270-93_270-90del
NR_045828.1:n.305-93_305-90del (APOM)
XM_006715150.2:c.174-93_174-90del (APOM) XP_006715213.1:n.174-93_174-90del
XM_011514895.1:c.-14+3189_-14+3192del (BAG6) XP_011513197.1:n.-14+3189_-14+3192del
XM_006715150.3:c.174-93_174-90del (APOM) XP_006715213.1:n.174-93_174-90del
XM_017011279.2:c.-14+3189_-14+3192del (BAG6) XP_016866768.1:n.-14+3189_-14+3192del
XM_024446545.1:c.-14+632_-14+635del (BAG6) XP_024302313.1:n.-14+632_-14+635del
NM_019101.3:c.270-93_270-90del (APOM) MANE Select NP_061974.2:n.270-93_270-90del
NM_001256169.2:c.54-93_54-90del (APOM) NP_001243098.1:n.54-93_54-90del
NR_045828.2:n.311-93_311-90del (APOM)