Canonical Allele Identifier: CA419401484
Gene: ALX3 HGNC NCBI
STRIP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.110607212T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110064590T>C , CM000663.2:g.110064590T>C GRCh38
NC_000001.10:g.110607212T>C , CM000663.1:g.110607212T>C GRCh37
NC_000001.9:g.110408735T>C NCBI36
NG_012039.1:g.11111A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647563.2:c.591A>G (ALX3) MANE Select ENSP00000497310.1:p.Val197=
ENST00000649954.1:c.162A>G (ALX3) ENSP00000497035.1:p.Val54=
ENST00000369792.4:c.591A>G (ALX3) ENSP00000358807.3:p.Val197=
ENST00000473429.5:n.4214-7865T>C (STRIP1)
NM_006492.2:c.591A>G (ALX3) NP_006483.2:p.Val197=
NM_006492.3:c.591A>G (ALX3) MANE Select NP_006483.2:p.Val197=
Search 100 bp 5'
Search 100 bp 3'