Canonical Allele Identifier: CA2768909827
Gene: ANXA6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151101042_151101043insCCCCAAACAC , CM000667.2:g.151101042_151101043insCCCCAAACAC GRCh38
NC_000005.9:g.150480603_150480604insCCCCAAACAC , CM000667.1:g.150480603_150480604insCCCCAAACAC GRCh37
NC_000005.8:g.150460796_150460797insCCCCAAACAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000354546.10:c.*406_*407insTGTTTGGGGG MANE Select ENSP00000346550.5:n.*406_*407insTGTTTGGGGG
ENST00000522664.5:c.201-80_201-79insTGTTTGGGGG
NM_001155.4:c.*406_*407insTGTTTGGGGG NP_001146.2:n.*406_*407insTGTTTGGGGG
NM_001193544.1:c.*406_*407insTGTTTGGGGG NP_001180473.1:n.*406_*407insTGTTTGGGGG
NM_001363114.1:c.*406_*407insTGTTTGGGGG NP_001350043.1:n.*406_*407insTGTTTGGGGG
NM_001155.5:c.*406_*407insTGTTTGGGGG MANE Select NP_001146.2:n.*406_*407insTGTTTGGGGG
NM_001193544.2:c.*406_*407insTGTTTGGGGG NP_001180473.1:n.*406_*407insTGTTTGGGGG
NM_001363114.2:c.*406_*407insTGTTTGGGGG NP_001350043.1:n.*406_*407insTGTTTGGGGG