Canonical Allele Identifier: CA1188354874
Gene: ALX3 HGNC NCBI
STRIP1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110064520C= , CM000663.2:g.110064520C= GRCh38
NC_000001.10:g.110607142C= , CM000663.1:g.110607142C= GRCh37
NC_000001.9:g.110408665C= NCBI36
NG_012039.1:g.11181G=

Transcript Alleles

HGVS Amino-acid change
ENST00000647563.2:c.594+67G= (ALX3) MANE Select ENSP00000497310.1:n.594+67G=
ENST00000649954.1:c.165+67G= (ALX3) ENSP00000497035.1:n.165+67G=
ENST00000369792.4:c.594+67G= (ALX3) ENSP00000358807.3:n.594+67G=
ENST00000473429.5:n.4214-7935C= (STRIP1)
NM_006492.2:c.594+67G= (ALX3) NP_006483.2:n.594+67G=
NM_006492.3:c.594+67G= (ALX3) MANE Select NP_006483.2:n.594+67G=
Search 100 bp 5'
Search 100 bp 3'