Canonical Allele Identifier: CA10638477
Gene: ALX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 304608
ClinVar RCV Id: RCV000288554
dbSNP Id: rs560087261
gnomAD v2: 11-44282299-G-A
gnomAD v3: 11-44260749-G-A
gnomAD v4: 11-44260749-G-A
MyVariant Identifiers: chr11:g.44282299G>A (hg19) chr11:g.44260749G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44260749G>A , CM000673.2:g.44260749G>A GRCh38
NC_000011.9:g.44282299G>A , CM000673.1:g.44282299G>A GRCh37
NC_000011.8:g.44238875G>A NCBI36
NG_015809.1:g.54418C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000652299.1:c.*4105C>T MANE Select ENSP00000498217.1:n.*4105C>T
ENST00000329255.3:c.*4105C>T ENSP00000332744.3:n.*4105C>T
NM_021926.3:c.*4105C>T NP_068745.2:n.*4105C>T
XM_011520265.1:c.*4105C>T XP_011518567.1:n.*4105C>T
XM_011520266.1:c.*4105C>T XP_011518568.1:n.*4105C>T
NM_021926.4:c.*4105C>T MANE Select NP_068745.2:n.*4105C>T
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