Canonical Allele Identifier: CA1435013367
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs1737933965
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862298dup , CM000666.2:g.4862298dup GRCh38
NC_000004.11:g.4864025dup , CM000666.1:g.4864025dup GRCh37
NC_000004.10:g.4914926dup NCBI36
NG_008121.1:g.7634dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.470-403dup MANE Select ENSP00000372170.4:n.470-403dup
ENST00000382723.4:c.470-403dup ENSP00000372170.4:n.470-403dup
NM_002448.3:c.470-403dup MANE Select NP_002439.2:n.470-403dup
Search 100 bp 5'
Search 100 bp 3'