Canonical Allele Identifier: CA1435013357
Gene: MSX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862276G= , CM000666.2:g.4862276G= GRCh38
NC_000004.11:g.4864003G= , CM000666.1:g.4864003G= GRCh37
NC_000004.10:g.4914904G= NCBI36
NG_008121.1:g.7612G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.470-425G= MANE Select ENSP00000372170.4:n.470-425G=
ENST00000382723.4:c.470-425G= ENSP00000372170.4:n.470-425G=
NM_002448.3:c.470-425G= MANE Select NP_002439.2:n.470-425G=
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