Canonical Allele Identifier: CA1435013644
Gene: MSX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862770C= , CM000666.2:g.4862770C= GRCh38
NC_000004.11:g.4864497C= , CM000666.1:g.4864497C= GRCh37
NC_000004.10:g.4915398C= NCBI36
NG_008121.1:g.8106C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.539C= MANE Select ENSP00000372170.4:p.Thr180=
ENST00000382723.4:c.539C= ENSP00000372170.4:p.Thr180=
ENST00000468421.1:n.251C=
NM_002448.3:c.539C= MANE Select NP_002439.2:p.Thr180=
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