Canonical Allele Identifier: CA124431
Gene: MSX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4860264G>A , CM000666.2:g.4860264G>A GRCh38
NC_000004.11:g.4861991G>A , CM000666.1:g.4861991G>A GRCh37
NC_000004.10:g.4912892G>A NCBI36
NG_008121.1:g.5600G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.365G>A MANE Select ENSP00000372170.4:p.Gly122Glu
ENST00000382723.4:c.365G>A ENSP00000372170.4:p.Gly122Glu
NM_002448.3:c.365G>A MANE Select NP_002439.2:p.Gly122Glu