Canonical Allele Identifier: CA1435013802
Gene: MSX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863105A= , CM000666.2:g.4863105A= GRCh38
NC_000004.11:g.4864832A= , CM000666.1:g.4864832A= GRCh37
NC_000004.10:g.4915733A= NCBI36
NG_008121.1:g.8441A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.874A= MANE Select ENSP00000372170.4:p.Thr292=
ENST00000382723.4:c.874A= ENSP00000372170.4:p.Thr292=
NM_002448.3:c.874A= MANE Select NP_002439.2:p.Thr292=