Canonical Allele Identifier: CA1602345353

Gene: MSX2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174724690T= , CM000667.2:g.174724690T=	GRCh38
NC_000005.9:g.174151693T= , CM000667.1:g.174151693T=	GRCh37
NC_000005.8:g.174084299T=	NCBI36
NG_008124.1:g.5119T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239243.7:c.31T= MANE Select	ENSP00000239243.5:p.Phe11=
ENST00000239243.6:c.31T=	ENSP00000239243.5:p.Phe11=
ENST00000507785.2:c.31T=	ENSP00000427425.1:p.Phe11=
NM_002449.4:c.31T=	NP_002440.2:p.Phe11=
NM_001363626.1:c.31T=	NP_001350555.1:p.Phe11=
NM_002449.5:c.31T= MANE Select	NP_002440.2:p.Phe11=
NM_001363626.2:c.31T=	NP_001350555.1:p.Phe11=