Canonical Allele Identifier: CA356138784
Gene: MSX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862983T>G , CM000666.2:g.4862983T>G GRCh38
NC_000004.11:g.4864710T>G , CM000666.1:g.4864710T>G GRCh37
NC_000004.10:g.4915611T>G NCBI36
NG_008121.1:g.8319T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.752T>G MANE Select ENSP00000372170.4:p.Phe251Cys
ENST00000382723.4:c.752T>G ENSP00000372170.4:p.Phe251Cys
ENST00000468421.1:n.464T>G
NM_002448.3:c.752T>G MANE Select NP_002439.2:p.Phe251Cys