Canonical Allele Identifier: CA1435013359
Gene: MSX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862283C= , CM000666.2:g.4862283C= GRCh38
NC_000004.11:g.4864010C= , CM000666.1:g.4864010C= GRCh37
NC_000004.10:g.4914911C= NCBI36
NG_008121.1:g.7619C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.470-418C= MANE Select ENSP00000372170.4:n.470-418C=
ENST00000382723.4:c.470-418C= ENSP00000372170.4:n.470-418C=
NM_002448.3:c.470-418C= MANE Select NP_002439.2:n.470-418C=
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