Canonical Allele Identifier: CA356137808

Gene: MSX1

Linked Data

• MyVariant Identifiers: chr4:g.4861970T>A (hg19) ; chr4:g.4860243T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.4860243T>A , CM000666.2:g.4860243T>A	GRCh38
NC_000004.11:g.4861970T>A , CM000666.1:g.4861970T>A	GRCh37
NC_000004.10:g.4912871T>A	NCBI36
NG_008121.1:g.5579T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000382723.5:c.344T>A MANE Select	ENSP00000372170.4:p.Leu115His
ENST00000382723.4:c.344T>A	ENSP00000372170.4:p.Leu115His
NM_002448.3:c.344T>A MANE Select	NP_002439.2:p.Leu115His