Canonical Allele Identifier: CA1602356128

Gene: MSX2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174729296G= , CM000667.2:g.174729296G=	GRCh38
NC_000005.9:g.174156299G= , CM000667.1:g.174156299G=	GRCh37
NC_000005.8:g.174088905G=	NCBI36
NG_008124.1:g.9725G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000239243.7:c.517G= MANE Select	ENSP00000239243.5:p.Ala173=
ENST00000239243.6:c.517G=	ENSP00000239243.5:p.Ala173=
ENST00000507785.2:c.*141G=	ENSP00000427425.1:n.*141G=
NM_002449.4:c.517G=	NP_002440.2:p.Ala173=
NM_001363626.1:c.*141G=	NP_001350555.1:n.*141G=
NM_002449.5:c.517G= MANE Select	NP_002440.2:p.Ala173=
NM_001363626.2:c.*141G=	NP_001350555.1:n.*141G=