Canonical Allele Identifier: CA997525
Gene: ALX3 HGNC NCBI
STRIP1 HGNC NCBI

Linked Data

dbSNP Id: rs748725555
ExAC: 1:110604084 C / G
MyVariant Identifiers: chr1:g.110604084C>G (hg19) chr1:g.110061462C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110061462C>G , CM000663.2:g.110061462C>G GRCh38
NC_000001.10:g.110604084C>G , CM000663.1:g.110604084C>G GRCh37
NC_000001.9:g.110405607C>G NCBI36
NG_012039.1:g.14239G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647563.2:c.696G>C (ALX3) MANE Select ENSP00000497310.1:p.Val232=
ENST00000649954.1:c.267G>C (ALX3) ENSP00000497035.1:p.Val89=
ENST00000369792.4:c.696G>C (ALX3) ENSP00000358807.3:p.Val232=
ENST00000473429.5:n.4213+6660C>G (STRIP1)
NM_006492.2:c.696G>C (ALX3) NP_006483.2:p.Val232=
NM_006492.3:c.696G>C (ALX3) MANE Select NP_006483.2:p.Val232=
Search 100 bp 5'
Search 100 bp 3'