Canonical Allele Identifier: CA380182223
Gene: ALX4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.44296942C>T (hg19) chr11:g.44275392C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44275392C>T , CM000673.2:g.44275392C>T GRCh38
NC_000011.9:g.44296942C>T , CM000673.1:g.44296942C>T GRCh37
NC_000011.8:g.44253518C>T NCBI36
NG_015809.1:g.39775G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000652299.1:c.733G>A MANE Select ENSP00000498217.1:p.Glu245Lys
ENST00000329255.3:c.733G>A ENSP00000332744.3:p.Glu245Lys
NM_021926.3:c.733G>A NP_068745.2:p.Glu245Lys
XM_011520264.1:c.733G>A XP_011518566.1:p.Glu245Lys
XM_011520265.1:c.211G>A XP_011518567.1:p.Glu71Lys
XM_011520266.1:c.211G>A XP_011518568.1:p.Glu71Lys
NM_021926.4:c.733G>A MANE Select NP_068745.2:p.Glu245Lys
Search 100 bp 5'
Search 100 bp 3'