Canonical Allele Identifier: CA380182218
Gene: ALX4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.44296941T>A (hg19) chr11:g.44275391T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44275391T>A , CM000673.2:g.44275391T>A GRCh38
NC_000011.9:g.44296941T>A , CM000673.1:g.44296941T>A GRCh37
NC_000011.8:g.44253517T>A NCBI36
NG_015809.1:g.39776A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000652299.1:c.734A>T MANE Select ENSP00000498217.1:p.Glu245Val
ENST00000329255.3:c.734A>T ENSP00000332744.3:p.Glu245Val
NM_021926.3:c.734A>T NP_068745.2:p.Glu245Val
XM_011520264.1:c.734A>T XP_011518566.1:p.Glu245Val
XM_011520265.1:c.212A>T XP_011518567.1:p.Glu71Val
XM_011520266.1:c.212A>T XP_011518568.1:p.Glu71Val
NM_021926.4:c.734A>T MANE Select NP_068745.2:p.Glu245Val
Search 100 bp 5'
Search 100 bp 3'