Canonical Allele Identifier: CA2669788698
Gene: MSX1 HGNC NCBI

Linked Data

gnomAD v4: 4-4863267-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863268del , CM000666.2:g.4863268del GRCh38
NC_000004.11:g.4864995del , CM000666.1:g.4864995del GRCh37
NC_000004.10:g.4915896del NCBI36
NG_008121.1:g.8604del

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.*125del MANE Select ENSP00000372170.4:n.*125del
ENST00000382723.4:c.*125del ENSP00000372170.4:n.*125del
NM_002448.3:c.*125del MANE Select NP_002439.2:n.*125del
Search 100 bp 5'
Search 100 bp 3'