Canonical Allele Identifier: CA1188354883

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110064536_110064537delinsTC , CM000663.2:g.110064536_110064537delinsTC GRCh38
NC_000001.10:g.110607158_110607159delinsTC , CM000663.1:g.110607158_110607159delinsTC GRCh37
NC_000001.9:g.110408681_110408682delinsTC NCBI36
NG_012039.1:g.11164_11165delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000647563.2:c.594+50_594+51delinsGA (ALX3) MANE Select ENSP00000497310.1:n.594+50_594+51delinsGA
ENST00000649954.1:c.165+50_165+51delinsGA (ALX3) ENSP00000497035.1:n.165+50_165+51delinsGA
ENST00000369792.4:c.594+50_594+51delinsGA (ALX3) ENSP00000358807.3:n.594+50_594+51delinsGA
ENST00000473429.5:n.4214-7919_4214-7918delinsTC (STRIP1)
NM_006492.2:c.594+50_594+51delinsGA (ALX3) NP_006483.2:n.594+50_594+51delinsGA
NM_006492.3:c.594+50_594+51delinsGA (ALX3) MANE Select NP_006483.2:n.594+50_594+51delinsGA