Canonical Allele Identifier: CA2768909832
Gene: ANXA6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151101086_151101087insCACCC , CM000667.2:g.151101086_151101087insCACCC GRCh38
NC_000005.9:g.150480647_150480648insCACCC , CM000667.1:g.150480647_150480648insCACCC GRCh37
NC_000005.8:g.150460840_150460841insCACCC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000354546.10:c.*361_*362insGGGTG MANE Select ENSP00000346550.5:n.*361_*362insGGGTG
ENST00000522664.5:c.201-125_201-124insGGGTG
NM_001155.4:c.*361_*362insGGGTG NP_001146.2:n.*361_*362insGGGTG
NM_001193544.1:c.*361_*362insGGGTG NP_001180473.1:n.*361_*362insGGGTG
NM_001363114.1:c.*361_*362insGGGTG NP_001350043.1:n.*361_*362insGGGTG
NM_001155.5:c.*361_*362insGGGTG MANE Select NP_001146.2:n.*361_*362insGGGTG
NM_001193544.2:c.*361_*362insGGGTG NP_001180473.1:n.*361_*362insGGGTG
NM_001363114.2:c.*361_*362insGGGTG NP_001350043.1:n.*361_*362insGGGTG