Canonical Allele Identifier: CA380181680
Gene: ALX4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.44286665G>C (hg19) chr11:g.44265115G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44265115G>C , CM000673.2:g.44265115G>C GRCh38
NC_000011.9:g.44286665G>C , CM000673.1:g.44286665G>C GRCh37
NC_000011.8:g.44243241G>C NCBI36
NG_015809.1:g.50052C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000652299.1:c.975C>G MANE Select ENSP00000498217.1:p.Cys325Trp
ENST00000329255.3:c.975C>G ENSP00000332744.3:p.Cys325Trp
NM_021926.3:c.975C>G NP_068745.2:p.Cys325Trp
XM_011520265.1:c.453C>G XP_011518567.1:p.Cys151Trp
XM_011520266.1:c.453C>G XP_011518568.1:p.Cys151Trp
NM_021926.4:c.975C>G MANE Select NP_068745.2:p.Cys325Trp
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