Canonical Allele Identifier: CA1435013557
Gene: MSX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862644A= , CM000666.2:g.4862644A= GRCh38
NC_000004.11:g.4864371A= , CM000666.1:g.4864371A= GRCh37
NC_000004.10:g.4915272A= NCBI36
NG_008121.1:g.7980A=

Transcript Alleles

HGVS Amino-acid change
ENST00000382723.5:c.470-57A= MANE Select ENSP00000372170.4:n.470-57A=
ENST00000382723.4:c.470-57A= ENSP00000372170.4:n.470-57A=
ENST00000468421.1:n.181+36A=
NM_002448.3:c.470-57A= MANE Select NP_002439.2:n.470-57A=