Canonical Allele Identifier: CA356139156
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs1737961323

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863094T>A , CM000666.2:g.4863094T>A GRCh38
NC_000004.11:g.4864821T>A , CM000666.1:g.4864821T>A GRCh37
NC_000004.10:g.4915722T>A NCBI36
NG_008121.1:g.8430T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.863T>A MANE Select ENSP00000372170.4:p.Val288Glu
ENST00000382723.4:c.863T>A ENSP00000372170.4:p.Val288Glu
NM_002448.3:c.863T>A MANE Select NP_002439.2:p.Val288Glu