Canonical Allele Identifier: CA1435013911
Gene: MSX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863279T= , CM000666.2:g.4863279T= GRCh38
NC_000004.11:g.4865006T= , CM000666.1:g.4865006T= GRCh37
NC_000004.10:g.4915907T= NCBI36
NG_008121.1:g.8615T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.*136T= MANE Select ENSP00000372170.4:n.*136T=
ENST00000382723.4:c.*136T= ENSP00000372170.4:n.*136T=
NM_002448.3:c.*136T= MANE Select NP_002439.2:n.*136T=
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