Canonical Allele Identifier: CA1967928927
Gene: ALX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44275386G= , CM000673.2:g.44275386G= GRCh38
NC_000011.9:g.44296936G= , CM000673.1:g.44296936G= GRCh37
NC_000011.8:g.44253512G= NCBI36
NG_015809.1:g.39781C=

Transcript Alleles

HGVS Amino-acid change
ENST00000652299.1:c.739C= MANE Select ENSP00000498217.1:p.Leu247=
ENST00000329255.3:c.739C= ENSP00000332744.3:p.Leu247=
NM_021926.3:c.739C= NP_068745.2:p.Leu247=
XM_011520264.1:c.739C= XP_011518566.1:p.Leu247=
XM_011520265.1:c.217C= XP_011518567.1:p.Leu73=
XM_011520266.1:c.217C= XP_011518568.1:p.Leu73=
NM_021926.4:c.739C= MANE Select NP_068745.2:p.Leu247=