Canonical Allele Identifier: CA10638578
Gene: ALX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 304689
ClinVar RCV Id: RCV000322118
dbSNP Id: rs113592690
gnomAD v2: 11-44285979-A-AG
gnomAD v3: 11-44264429-A-AG
gnomAD v4: 11-44264429-A-AG
MyVariant Identifiers: chr11:g.44285980dupG (hg19) chr11:g.44285979_44285980insG (hg19) chr11:g.44264430dupG (hg38) chr11:g.44264429_44264430insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44264433dup , CM000673.2:g.44264433dup GRCh38
NC_000011.9:g.44285983dup , CM000673.1:g.44285983dup GRCh37
NC_000011.8:g.44242559dup NCBI36
NG_015809.1:g.50737dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000652299.1:c.*424dup MANE Select ENSP00000498217.1:n.*424dup
ENST00000329255.3:c.*424dup ENSP00000332744.3:n.*424dup
NM_021926.3:c.*424dup NP_068745.2:n.*424dup
XM_011520265.1:c.*424dup XP_011518567.1:n.*424dup
XM_011520266.1:c.*424dup XP_011518568.1:n.*424dup
NM_021926.4:c.*424dup MANE Select NP_068745.2:n.*424dup
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