Canonical Allele Identifier: CA1435013578
Gene: MSX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862668A= , CM000666.2:g.4862668A= GRCh38
NC_000004.11:g.4864395A= , CM000666.1:g.4864395A= GRCh37
NC_000004.10:g.4915296A= NCBI36
NG_008121.1:g.8004A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.470-33A= MANE Select ENSP00000372170.4:n.470-33A=
ENST00000382723.4:c.470-33A= ENSP00000372170.4:n.470-33A=
ENST00000468421.1:n.182-33A=
NM_002448.3:c.470-33A= MANE Select NP_002439.2:n.470-33A=