Canonical Allele Identifier: CA91672666
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs906845052
gnomAD v3: 4-4863254-C-CA
gnomAD v4: 4-4863254-C-CA
MyVariant Identifiers: chr4:g.4864981_4864982insA (hg19) chr4:g.4863254_4863255insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863255dup , CM000666.2:g.4863255dup GRCh38
NC_000004.11:g.4864982dup , CM000666.1:g.4864982dup GRCh37
NC_000004.10:g.4915883dup NCBI36
NG_008121.1:g.8591dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.*112dup MANE Select ENSP00000372170.4:n.*112dup
ENST00000382723.4:c.*112dup ENSP00000372170.4:n.*112dup
NM_002448.3:c.*112dup MANE Select NP_002439.2:n.*112dup
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Search 100 bp 3'