Canonical Allele Identifier: CA1435013838
Gene: MSX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863168G= , CM000666.2:g.4863168G= GRCh38
NC_000004.11:g.4864895G= , CM000666.1:g.4864895G= GRCh37
NC_000004.10:g.4915796G= NCBI36
NG_008121.1:g.8504G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.*25G= MANE Select ENSP00000372170.4:n.*25G=
ENST00000382723.4:c.*25G= ENSP00000372170.4:n.*25G=
NM_002448.3:c.*25G= MANE Select NP_002439.2:n.*25G=