Canonical Allele Identifier: CA1435013886
Gene: MSX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863234C= , CM000666.2:g.4863234C= GRCh38
NC_000004.11:g.4864961C= , CM000666.1:g.4864961C= GRCh37
NC_000004.10:g.4915862C= NCBI36
NG_008121.1:g.8570C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.*91C= MANE Select ENSP00000372170.4:n.*91C=
ENST00000382723.4:c.*91C= ENSP00000372170.4:n.*91C=
NM_002448.3:c.*91C= MANE Select NP_002439.2:n.*91C=
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