Canonical Allele Identifier: CA566364003

Linked Data

dbSNP Id: rs1278608173

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657144_31657145insA , CM000668.2:g.31657144_31657145insA GRCh38
NC_000006.11:g.31624921_31624922insA , CM000668.1:g.31624921_31624922insA GRCh37
NC_000006.10:g.31732900_31732901insA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.270-81_270-80insA (APOM) MANE Select ENSP00000365081.3:n.270-81_270-80insA
ENST00000375916.3:c.270-81_270-80insA (APOM) ENSP00000365081.3:n.270-81_270-80insA
ENST00000375918.6:c.54-81_54-80insA (APOM) ENSP00000365083.2:n.54-81_54-80insA
ENST00000375920.8:c.54-81_54-80insA (APOM) ENSP00000365085.4:n.54-81_54-80insA
NM_001256169.1:c.54-81_54-80insA (APOM) NP_001243098.1:n.54-81_54-80insA
NM_019101.2:c.270-81_270-80insA (APOM) NP_061974.2:n.270-81_270-80insA
NR_045828.1:n.305-81_305-80insA (APOM)
XM_006715150.2:c.174-81_174-80insA (APOM) XP_006715213.1:n.174-81_174-80insA
XM_011514895.1:c.-14+3176_-14+3177insT (BAG6) XP_011513197.1:n.-14+3176_-14+3177insT
XM_006715150.3:c.174-81_174-80insA (APOM) XP_006715213.1:n.174-81_174-80insA
XM_017011279.2:c.-14+3176_-14+3177insT (BAG6) XP_016866768.1:n.-14+3176_-14+3177insT
XM_024446545.1:c.-14+619_-14+620insT (BAG6) XP_024302313.1:n.-14+619_-14+620insT
NM_019101.3:c.270-81_270-80insA (APOM) MANE Select NP_061974.2:n.270-81_270-80insA
NM_001256169.2:c.54-81_54-80insA (APOM) NP_001243098.1:n.54-81_54-80insA
NR_045828.2:n.311-81_311-80insA (APOM)