Canonical Allele Identifier: CA2740501451
Gene: MSX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862676G>T , CM000666.2:g.4862676G>T GRCh38
NC_000004.11:g.4864403G>T , CM000666.1:g.4864403G>T GRCh37
NC_000004.10:g.4915304G>T NCBI36
NG_008121.1:g.8012G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.470-25G>T MANE Select ENSP00000372170.4:n.470-25G>T
ENST00000382723.4:c.470-25G>T ENSP00000372170.4:n.470-25G>T
ENST00000468421.1:n.182-25G>T
NM_002448.3:c.470-25G>T MANE Select NP_002439.2:n.470-25G>T