Canonical Allele Identifier: CA1435012150
Gene: MSX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4860155G= , CM000666.2:g.4860155G= GRCh38
NC_000004.11:g.4861882G= , CM000666.1:g.4861882G= GRCh37
NC_000004.10:g.4912783G= NCBI36
NG_008121.1:g.5491G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.256G= MANE Select ENSP00000372170.4:p.Val86=
ENST00000382723.4:c.256G= ENSP00000372170.4:p.Val86=
NM_002448.3:c.256G= MANE Select NP_002439.2:p.Val86=