Canonical Allele Identifier: CA1435013404
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs1737935579

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862366_4862400del , CM000666.2:g.4862366_4862400del GRCh38
NC_000004.11:g.4864093_4864127del , CM000666.1:g.4864093_4864127del GRCh37
NC_000004.10:g.4914994_4915028del NCBI36
NG_008121.1:g.7702_7736del

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.470-335_470-301del MANE Select ENSP00000372170.4:n.470-335_470-301del
ENST00000382723.4:c.470-335_470-301del ENSP00000372170.4:n.470-335_470-301del
NM_002448.3:c.470-335_470-301del MANE Select NP_002439.2:n.470-335_470-301del