Canonical Allele Identifier: CA2586973680
Gene: MSX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863128_4863129del , CM000666.2:g.4863128_4863129del GRCh38
NC_000004.11:g.4864855_4864856del , CM000666.1:g.4864855_4864856del GRCh37
NC_000004.10:g.4915756_4915757del NCBI36
NG_008121.1:g.8464_8465del

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.897_898del MANE Select ENSP00000372170.4:p.Met299IlefsTer?
ENST00000382723.4:c.897_898del ENSP00000372170.4:p.Met299IlefsTer?
NM_002448.3:c.897_898del MANE Select NP_002439.2:p.Met299IlefsTer?