Canonical Allele Identifier: CA1435013613
Gene: MSX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862710_4862711delinsGC , CM000666.2:g.4862710_4862711delinsGC GRCh38
NC_000004.11:g.4864437_4864438delinsGC , CM000666.1:g.4864437_4864438delinsGC GRCh37
NC_000004.10:g.4915338_4915339delinsGC NCBI36
NG_008121.1:g.8046_8047delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000382723.5:c.479_480delinsGC MANE Select ENSP00000372170.4:p.Ser160=
ENST00000382723.4:c.479_480delinsGC ENSP00000372170.4:p.Ser160=
ENST00000468421.1:n.191_192delinsGC
NM_002448.3:c.479_480delinsGC MANE Select NP_002439.2:p.Ser160=