Canonical Allele Identifier: CA1435013366
Gene: MSX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862297C= , CM000666.2:g.4862297C= GRCh38
NC_000004.11:g.4864024C= , CM000666.1:g.4864024C= GRCh37
NC_000004.10:g.4914925C= NCBI36
NG_008121.1:g.7633C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.470-404C= MANE Select ENSP00000372170.4:n.470-404C=
ENST00000382723.4:c.470-404C= ENSP00000372170.4:n.470-404C=
NM_002448.3:c.470-404C= MANE Select NP_002439.2:n.470-404C=
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