Canonical Allele Identifier: CA1435013663
Gene: MSX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862812A= , CM000666.2:g.4862812A= GRCh38
NC_000004.11:g.4864539A= , CM000666.1:g.4864539A= GRCh37
NC_000004.10:g.4915440A= NCBI36
NG_008121.1:g.8148A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.581A= MANE Select ENSP00000372170.4:p.Lys194=
ENST00000382723.4:c.581A= ENSP00000372170.4:p.Lys194=
ENST00000468421.1:n.293A=
NM_002448.3:c.581A= MANE Select NP_002439.2:p.Lys194=
Search 100 bp 5'
Search 100 bp 3'