Canonical Allele Identifier: CA1435012240
Gene: MSX1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4860292C= , CM000666.2:g.4860292C= GRCh38
NC_000004.11:g.4862019C= , CM000666.1:g.4862019C= GRCh37
NC_000004.10:g.4912920C= NCBI36
NG_008121.1:g.5628C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.393C= MANE Select ENSP00000372170.4:p.Leu131=
ENST00000382723.4:c.393C= ENSP00000372170.4:p.Leu131=
NM_002448.3:c.393C= MANE Select NP_002439.2:p.Leu131=
Search 100 bp 5'
Search 100 bp 3'