Canonical Allele Identifier: CA2705103468
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs2108778369
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862261_4862263del , CM000666.2:g.4862261_4862263del GRCh38
NC_000004.11:g.4863988_4863990del , CM000666.1:g.4863988_4863990del GRCh37
NC_000004.10:g.4914889_4914891del NCBI36
NG_008121.1:g.7597_7599del

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.470-440_470-438del MANE Select ENSP00000372170.4:n.470-440_470-438del
ENST00000382723.4:c.470-440_470-438del ENSP00000372170.4:n.470-440_470-438del
NM_002448.3:c.470-440_470-438del MANE Select NP_002439.2:n.470-440_470-438del
Search 100 bp 5'
Search 100 bp 3'