Canonical Allele Identifier: CA1602356122

Gene: MSX2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174729295T= , CM000667.2:g.174729295T=	GRCh38
NC_000005.9:g.174156298T= , CM000667.1:g.174156298T=	GRCh37
NC_000005.8:g.174088904T=	NCBI36
NG_008124.1:g.9724T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000239243.7:c.516T= MANE Select	ENSP00000239243.5:p.Arg172=
ENST00000239243.6:c.516T=	ENSP00000239243.5:p.Arg172=
ENST00000507785.2:c.*140T=	ENSP00000427425.1:n.*140T=
NM_002449.4:c.516T=	NP_002440.2:p.Arg172=
NM_001363626.1:c.*140T=	NP_001350555.1:n.*140T=
NM_002449.5:c.516T= MANE Select	NP_002440.2:p.Arg172=
NM_001363626.2:c.*140T=	NP_001350555.1:n.*140T=