Canonical Allele Identifier: CA10634884
Gene: ALX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 304666
ClinVar RCV Id: RCV000331487
dbSNP Id: rs886048303
gnomAD v3: 11-44263719-G-A
gnomAD v4: 11-44263719-G-A
MyVariant Identifiers: chr11:g.44285269G>A (hg19) chr11:g.44263719G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44263719G>A , CM000673.2:g.44263719G>A GRCh38
NC_000011.9:g.44285269G>A , CM000673.1:g.44285269G>A GRCh37
NC_000011.8:g.44241845G>A NCBI36
NG_015809.1:g.51448C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000652299.1:c.*1135C>T MANE Select ENSP00000498217.1:n.*1135C>T
ENST00000329255.3:c.*1135C>T ENSP00000332744.3:n.*1135C>T
NM_021926.3:c.*1135C>T NP_068745.2:n.*1135C>T
XM_011520265.1:c.*1135C>T XP_011518567.1:n.*1135C>T
XM_011520266.1:c.*1135C>T XP_011518568.1:n.*1135C>T
NM_021926.4:c.*1135C>T MANE Select NP_068745.2:n.*1135C>T
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