Canonical Allele Identifier: CA2760244104
Gene: MSX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863178T>G , CM000666.2:g.4863178T>G GRCh38
NC_000004.11:g.4864905T>G , CM000666.1:g.4864905T>G GRCh37
NC_000004.10:g.4915806T>G NCBI36
NG_008121.1:g.8514T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.*35T>G MANE Select ENSP00000372170.4:n.*35T>G
ENST00000382723.4:c.*35T>G ENSP00000372170.4:n.*35T>G
NM_002448.3:c.*35T>G MANE Select NP_002439.2:n.*35T>G