Canonical Allele Identifier: CA221484002
Gene: ALX4 HGNC NCBI
ClinVar RCV:
ClinVar Variation:
dbSNP:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44261449C>A , CM000673.2:g.44261449C>A GRCh38
NC_000011.9:g.44282999C>A , CM000673.1:g.44282999C>A GRCh37
NC_000011.8:g.44239575C>A NCBI36
NG_015809.1:g.53718G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000652299.1:c.*3405G>T MANE Select ENSP00000498217.1:n.*3405G>T
ENST00000329255.3:c.*3405G>T ENSP00000332744.3:n.*3405G>T
NM_021926.3:c.*3405G>T NP_068745.2:n.*3405G>T
XM_011520265.1:c.*3405G>T XP_011518567.1:n.*3405G>T
XM_011520266.1:c.*3405G>T XP_011518568.1:n.*3405G>T
NM_021926.4:c.*3405G>T MANE Select NP_068745.2:n.*3405G>T