Canonical Allele Identifier: CA1602356159

Gene: MSX2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174729318A= , CM000667.2:g.174729318A=	GRCh38
NC_000005.9:g.174156321A= , CM000667.1:g.174156321A=	GRCh37
NC_000005.8:g.174088927A=	NCBI36
NG_008124.1:g.9747A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239243.7:c.539A= MANE Select	ENSP00000239243.5:p.Asn180=
ENST00000239243.6:c.539A=	ENSP00000239243.5:p.Asn180=
ENST00000507785.2:c.*163A=	ENSP00000427425.1:n.*163A=
NM_002449.4:c.539A=	NP_002440.2:p.Asn180=
NM_001363626.1:c.*163A=	NP_001350555.1:n.*163A=
NM_002449.5:c.539A= MANE Select	NP_002440.2:p.Asn180=
NM_001363626.2:c.*163A=	NP_001350555.1:n.*163A=