Canonical Allele Identifier: CA1188354907
Gene: ALX3 HGNC NCBI
STRIP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110064584C= , CM000663.2:g.110064584C= GRCh38
NC_000001.10:g.110607206C= , CM000663.1:g.110607206C= GRCh37
NC_000001.9:g.110408729C= NCBI36
NG_012039.1:g.11117G=

Transcript Alleles

HGVS Amino-acid change
ENST00000647563.2:c.594+3G= (ALX3) MANE Select ENSP00000497310.1:n.594+3G=
ENST00000649954.1:c.165+3G= (ALX3) ENSP00000497035.1:n.165+3G=
ENST00000369792.4:c.594+3G= (ALX3) ENSP00000358807.3:n.594+3G=
ENST00000473429.5:n.4214-7871C= (STRIP1)
NM_006492.2:c.594+3G= (ALX3) NP_006483.2:n.594+3G=
NM_006492.3:c.594+3G= (ALX3) MANE Select NP_006483.2:n.594+3G=
Search 100 bp 5'
Search 100 bp 3'