Canonical Allele Identifier: CA2658868947
Gene: SIX3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.44942013_44942045del , CM000664.2:g.44942013_44942045del GRCh38
NC_000002.11:g.45169152_45169184del , CM000664.1:g.45169152_45169184del GRCh37
NC_000002.10:g.45022656_45022688del NCBI36
NG_016222.1:g.5116_5148del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260653.5:c.-92_-60del MANE Select ENSP00000260653.3:n.-92_-60del
ENST00000260653.4:c.-92_-60del ENSP00000260653.3:n.-92_-60del
NM_005413.3:c.-92_-60del NP_005404.1:n.-92_-60del
XM_011533042.1:c.-92_-60del XP_011531344.1:n.-92_-60del
NM_005413.4:c.-92_-60del MANE Select NP_005404.1:n.-92_-60del