Canonical Allele Identifier: CA1602346948

Gene: MSX2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174725082T= , CM000667.2:g.174725082T=	GRCh38
NC_000005.9:g.174152085T= , CM000667.1:g.174152085T=	GRCh37
NC_000005.8:g.174084691T=	NCBI36
NG_008124.1:g.5511T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239243.7:c.379+44T= MANE Select	ENSP00000239243.5:n.379+44T=
ENST00000239243.6:c.379+44T=	ENSP00000239243.5:n.379+44T=
ENST00000507785.2:c.*3+15T=	ENSP00000427425.1:n.*3+15T=
NM_002449.4:c.379+44T=	NP_002440.2:n.379+44T=
NM_001363626.1:c.*3+15T=	NP_001350555.1:n.*3+15T=
NM_002449.5:c.379+44T= MANE Select	NP_002440.2:n.379+44T=
NM_001363626.2:c.*3+15T=	NP_001350555.1:n.*3+15T=