Canonical Allele Identifier: CA380181685
Gene: ALX4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.44286667A>C (hg19) chr11:g.44265117A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44265117A>C , CM000673.2:g.44265117A>C GRCh38
NC_000011.9:g.44286667A>C , CM000673.1:g.44286667A>C GRCh37
NC_000011.8:g.44243243A>C NCBI36
NG_015809.1:g.50050T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000652299.1:c.973T>G MANE Select ENSP00000498217.1:p.Cys325Gly
ENST00000329255.3:c.973T>G ENSP00000332744.3:p.Cys325Gly
NM_021926.3:c.973T>G NP_068745.2:p.Cys325Gly
XM_011520265.1:c.451T>G XP_011518567.1:p.Cys151Gly
XM_011520266.1:c.451T>G XP_011518568.1:p.Cys151Gly
NM_021926.4:c.973T>G MANE Select NP_068745.2:p.Cys325Gly
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