Canonical Allele Identifier: CA1435013435
Gene: MSX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862425G= , CM000666.2:g.4862425G= GRCh38
NC_000004.11:g.4864152G= , CM000666.1:g.4864152G= GRCh37
NC_000004.10:g.4915053G= NCBI36
NG_008121.1:g.7761G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.470-276G= MANE Select ENSP00000372170.4:n.470-276G=
ENST00000382723.4:c.470-276G= ENSP00000372170.4:n.470-276G=
NM_002448.3:c.470-276G= MANE Select NP_002439.2:n.470-276G=