Canonical Allele Identifier: CA1602346873

Gene: MSX2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174725069T= , CM000667.2:g.174725069T=	GRCh38
NC_000005.9:g.174152072T= , CM000667.1:g.174152072T=	GRCh37
NC_000005.8:g.174084678T=	NCBI36
NG_008124.1:g.5498T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239243.7:c.379+31T= MANE Select	ENSP00000239243.5:n.379+31T=
ENST00000239243.6:c.379+31T=	ENSP00000239243.5:n.379+31T=
ENST00000507785.2:c.*3+2T=	ENSP00000427425.1:n.*3+2T=
NM_002449.4:c.379+31T=	NP_002440.2:n.379+31T=
NM_001363626.1:c.*3+2T=	NP_001350555.1:n.*3+2T=
NM_002449.5:c.379+31T= MANE Select	NP_002440.2:n.379+31T=
NM_001363626.2:c.*3+2T=	NP_001350555.1:n.*3+2T=