Canonical Allele Identifier: CA91671121
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs973409461
gnomAD v2: 4-4864017-C-CCT
gnomAD v4: 4-4862290-C-CCT
MyVariant Identifiers: chr4:g.4864017_4864018insCT (hg19) chr4:g.4862290_4862291insCT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862293_4862294dup , CM000666.2:g.4862293_4862294dup GRCh38
NC_000004.11:g.4864020_4864021dup , CM000666.1:g.4864020_4864021dup GRCh37
NC_000004.10:g.4914921_4914922dup NCBI36
NG_008121.1:g.7629_7630dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.470-408_470-407dup MANE Select ENSP00000372170.4:n.470-408_470-407dup
ENST00000382723.4:c.470-408_470-407dup ENSP00000372170.4:n.470-408_470-407dup
NM_002448.3:c.470-408_470-407dup MANE Select NP_002439.2:n.470-408_470-407dup
Search 100 bp 5'
Search 100 bp 3'