Canonical Allele Identifier: CA356139006

Gene: MSX1

Linked Data

• MyVariant Identifiers: chr4:g.4864790T>G (hg19) ; chr4:g.4863063T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.4863063T>G , CM000666.2:g.4863063T>G	GRCh38
NC_000004.11:g.4864790T>G , CM000666.1:g.4864790T>G	GRCh37
NC_000004.10:g.4915691T>G	NCBI36
NG_008121.1:g.8399T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382723.5:c.832T>G MANE Select	ENSP00000372170.4:p.Phe278Val
ENST00000382723.4:c.832T>G	ENSP00000372170.4:p.Phe278Val
NM_002448.3:c.832T>G MANE Select	NP_002439.2:p.Phe278Val