Canonical Allele Identifier: CA28739235

Linked Data

dbSNP Id: rs35647492

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110064470del , CM000663.2:g.110064470del GRCh38
NC_000001.10:g.110607092del , CM000663.1:g.110607092del GRCh37
NC_000001.9:g.110408615del NCBI36
NG_012039.1:g.11234del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647563.2:c.594+120del (ALX3) MANE Select ENSP00000497310.1:n.594+120del
ENST00000649954.1:c.165+120del (ALX3) ENSP00000497035.1:n.165+120del
ENST00000369792.4:c.594+120del (ALX3) ENSP00000358807.3:n.594+120del
ENST00000473429.5:n.4214-7985del (STRIP1)
NM_006492.2:c.594+120del (ALX3) NP_006483.2:n.594+120del
NM_006492.3:c.594+120del (ALX3) MANE Select NP_006483.2:n.594+120del