Canonical Allele Identifier: CA2677983173

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31656674_31656675del , CM000668.2:g.31656674_31656675del GRCh38
NC_000006.11:g.31624451_31624452del , CM000668.1:g.31624451_31624452del GRCh37
NC_000006.10:g.31732430_31732431del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375916.4:c.269+48_269+49del (APOM) MANE Select ENSP00000365081.3:n.269+48_269+49del
ENST00000375916.3:c.269+48_269+49del (APOM) ENSP00000365081.3:n.269+48_269+49del
ENST00000375918.6:c.53+48_53+49del (APOM) ENSP00000365083.2:n.53+48_53+49del
ENST00000375920.8:c.53+48_53+49del (APOM) ENSP00000365085.4:n.53+48_53+49del
NM_001256169.1:c.53+48_53+49del (APOM) NP_001243098.1:n.53+48_53+49del
NM_019101.2:c.269+48_269+49del (APOM) NP_061974.2:n.269+48_269+49del
NR_045828.1:n.304+41_304+42del (APOM)
XM_006715150.2:c.173+41_173+42del (APOM) XP_006715213.1:n.173+41_173+42del
XM_011514895.1:c.-14+3647_-14+3648del (BAG6) XP_011513197.1:n.-14+3647_-14+3648del
XM_006715150.3:c.173+41_173+42del (APOM) XP_006715213.1:n.173+41_173+42del
XM_017011279.2:c.-14+3647_-14+3648del (BAG6) XP_016866768.1:n.-14+3647_-14+3648del
XM_024446545.1:c.-14+1090_-14+1091del (BAG6) XP_024302313.1:n.-14+1090_-14+1091del
NM_019101.3:c.269+48_269+49del (APOM) MANE Select NP_061974.2:n.269+48_269+49del
NM_001256169.2:c.53+48_53+49del (APOM) NP_001243098.1:n.53+48_53+49del
NR_045828.2:n.310+41_310+42del (APOM)