Canonical Allele Identifier: CA10638523
Gene: ALX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 304637
ClinVar RCV Id: RCV000313720
dbSNP Id: rs886048292
gnomAD v4: 11-44262365-G-A
MyVariant Identifiers: chr11:g.44283915G>A (hg19) chr11:g.44262365G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44262365G>A , CM000673.2:g.44262365G>A GRCh38
NC_000011.9:g.44283915G>A , CM000673.1:g.44283915G>A GRCh37
NC_000011.8:g.44240491G>A NCBI36
NG_015809.1:g.52802C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000652299.1:c.*2489C>T MANE Select ENSP00000498217.1:n.*2489C>T
ENST00000329255.3:c.*2489C>T ENSP00000332744.3:n.*2489C>T
NM_021926.3:c.*2489C>T NP_068745.2:n.*2489C>T
XM_011520265.1:c.*2489C>T XP_011518567.1:n.*2489C>T
XM_011520266.1:c.*2489C>T XP_011518568.1:n.*2489C>T
NM_021926.4:c.*2489C>T MANE Select NP_068745.2:n.*2489C>T
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