Canonical Allele Identifier: CA1435013752
Gene: MSX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863028C= , CM000666.2:g.4863028C= GRCh38
NC_000004.11:g.4864755C= , CM000666.1:g.4864755C= GRCh37
NC_000004.10:g.4915656C= NCBI36
NG_008121.1:g.8364C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.797C= MANE Select ENSP00000372170.4:p.Ala266=
ENST00000382723.4:c.797C= ENSP00000372170.4:p.Ala266=
ENST00000468421.1:n.509C=
NM_002448.3:c.797C= MANE Select NP_002439.2:p.Ala266=