Canonical Allele Identifier: CA1602356178

Gene: MSX2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174729331C= , CM000667.2:g.174729331C=	GRCh38
NC_000005.9:g.174156334C= , CM000667.1:g.174156334C=	GRCh37
NC_000005.8:g.174088940C=	NCBI36
NG_008124.1:g.9760C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239243.7:c.552C= MANE Select	ENSP00000239243.5:p.Thr184=
ENST00000239243.6:c.552C=	ENSP00000239243.5:p.Thr184=
ENST00000507785.2:c.*176C=	ENSP00000427425.1:n.*176C=
NM_002449.4:c.552C=	NP_002440.2:p.Thr184=
NM_001363626.1:c.*176C=	NP_001350555.1:n.*176C=
NM_002449.5:c.552C= MANE Select	NP_002440.2:p.Thr184=
NM_001363626.2:c.*176C=	NP_001350555.1:n.*176C=