Canonical Allele Identifier: CA2499217211
Gene: MSX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1064708
ClinVar RCV Id: RCV001374733
dbSNP Id: rs2108778623

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862807_4862808insTAG , CM000666.2:g.4862807_4862808insTAG GRCh38
NC_000004.11:g.4864534_4864535insTAG , CM000666.1:g.4864534_4864535insTAG GRCh37
NC_000004.10:g.4915435_4915436insTAG NCBI36
NG_008121.1:g.8143_8144insTAG

Transcript Alleles

HGVS Amino-acid change
ENST00000382723.5:c.576_577insTAG
ENST00000382723.4:c.576_577insTAG
ENST00000468421.1:n.288_289insTAG
NM_002448.3:c.576_577insTAG