Canonical Allele Identifier: CA447978659

Gene: MSX2

Linked Data

• MyVariant Identifiers: chr5:g.174152016A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174725013A>G , CM000667.2:g.174725013A>G	GRCh38
NC_000005.9:g.174152016A>G , CM000667.1:g.174152016A>G	GRCh37
NC_000005.8:g.174084622A>G	NCBI36
NG_008124.1:g.5442A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239243.7:c.354A>G MANE Select	ENSP00000239243.5:p.Glu118=
ENST00000239243.6:c.354A>G	ENSP00000239243.5:p.Glu118=
ENST00000507785.2:c.354A>G	ENSP00000427425.1:p.Glu118=
NM_002449.4:c.354A>G	NP_002440.2:p.Glu118=
NM_001363626.1:c.354A>G	NP_001350555.1:p.Glu118=
NM_002449.5:c.354A>G MANE Select	NP_002440.2:p.Glu118=
NM_001363626.2:c.354A>G	NP_001350555.1:p.Glu118=