Canonical Allele Identifier: CA380181423
Gene: ALX4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.44286567T>A (hg19) chr11:g.44265017T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44265017T>A , CM000673.2:g.44265017T>A GRCh38
NC_000011.9:g.44286567T>A , CM000673.1:g.44286567T>A GRCh37
NC_000011.8:g.44243143T>A NCBI36
NG_015809.1:g.50150A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000652299.1:c.1073A>T MANE Select ENSP00000498217.1:p.His358Leu
ENST00000329255.3:c.1073A>T ENSP00000332744.3:p.His358Leu
NM_021926.3:c.1073A>T NP_068745.2:p.His358Leu
XM_011520265.1:c.551A>T XP_011518567.1:p.His184Leu
XM_011520266.1:c.551A>T XP_011518568.1:p.His184Leu
NM_021926.4:c.1073A>T MANE Select NP_068745.2:p.His358Leu
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