Canonical Allele Identifier: CA1435013782
Gene: MSX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863072G= , CM000666.2:g.4863072G= GRCh38
NC_000004.11:g.4864799G= , CM000666.1:g.4864799G= GRCh37
NC_000004.10:g.4915700G= NCBI36
NG_008121.1:g.8408G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.841G= MANE Select ENSP00000372170.4:p.Ala281=
ENST00000382723.4:c.841G= ENSP00000372170.4:p.Ala281=
NM_002448.3:c.841G= MANE Select NP_002439.2:p.Ala281=