Canonical Allele Identifier: CA1188354881

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110064533_110064535delinsTGG , CM000663.2:g.110064533_110064535delinsTGG GRCh38
NC_000001.10:g.110607155_110607157delinsTGG , CM000663.1:g.110607155_110607157delinsTGG GRCh37
NC_000001.9:g.110408678_110408680delinsTGG NCBI36
NG_012039.1:g.11166_11168delinsCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000647563.2:c.594+52_594+54delinsCCA (ALX3) MANE Select ENSP00000497310.1:n.594+52_594+54delinsCCA
ENST00000649954.1:c.165+52_165+54delinsCCA (ALX3) ENSP00000497035.1:n.165+52_165+54delinsCCA
ENST00000369792.4:c.594+52_594+54delinsCCA (ALX3) ENSP00000358807.3:n.594+52_594+54delinsCCA
ENST00000473429.5:n.4214-7922_4214-7920delinsTGG (STRIP1)
NM_006492.2:c.594+52_594+54delinsCCA (ALX3) NP_006483.2:n.594+52_594+54delinsCCA
NM_006492.3:c.594+52_594+54delinsCCA (ALX3) MANE Select NP_006483.2:n.594+52_594+54delinsCCA