Canonical Allele Identifier: CA1435013869
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs1737965354
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863206_4863210dup , CM000666.2:g.4863206_4863210dup GRCh38
NC_000004.11:g.4864933_4864937dup , CM000666.1:g.4864933_4864937dup GRCh37
NC_000004.10:g.4915834_4915838dup NCBI36
NG_008121.1:g.8542_8546dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.*63_*67dup MANE Select ENSP00000372170.4:n.*63_*67dup
ENST00000382723.4:c.*63_*67dup ENSP00000372170.4:n.*63_*67dup
NM_002448.3:c.*63_*67dup MANE Select NP_002439.2:n.*63_*67dup
Search 100 bp 5'
Search 100 bp 3'