Canonical Allele Identifier: CA1435013372
Gene: MSX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862307G= , CM000666.2:g.4862307G= GRCh38
NC_000004.11:g.4864034G= , CM000666.1:g.4864034G= GRCh37
NC_000004.10:g.4914935G= NCBI36
NG_008121.1:g.7643G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.470-394G= MANE Select ENSP00000372170.4:n.470-394G=
ENST00000382723.4:c.470-394G= ENSP00000372170.4:n.470-394G=
NM_002448.3:c.470-394G= MANE Select NP_002439.2:n.470-394G=
Search 100 bp 5'
Search 100 bp 3'