Canonical Allele Identifier: CA1435013776
Gene: MSX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863064T= , CM000666.2:g.4863064T= GRCh38
NC_000004.11:g.4864791T= , CM000666.1:g.4864791T= GRCh37
NC_000004.10:g.4915692T= NCBI36
NG_008121.1:g.8400T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.833T= MANE Select ENSP00000372170.4:p.Phe278=
ENST00000382723.4:c.833T= ENSP00000372170.4:p.Phe278=
NM_002448.3:c.833T= MANE Select NP_002439.2:p.Phe278=