Canonical Allele Identifier: CA1435013748
Gene: MSX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863018G= , CM000666.2:g.4863018G= GRCh38
NC_000004.11:g.4864745G= , CM000666.1:g.4864745G= GRCh37
NC_000004.10:g.4915646G= NCBI36
NG_008121.1:g.8354G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.787G= MANE Select ENSP00000372170.4:p.Val263=
ENST00000382723.4:c.787G= ENSP00000372170.4:p.Val263=
ENST00000468421.1:n.499G=
NM_002448.3:c.787G= MANE Select NP_002439.2:p.Val263=