Canonical Allele Identifier: CA1602345065

Gene: MSX2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174724606C= , CM000667.2:g.174724606C=	GRCh38
NC_000005.9:g.174151609C= , CM000667.1:g.174151609C=	GRCh37
NC_000005.8:g.174084215C=	NCBI36
NG_008124.1:g.5035C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239243.7:c.-54C= MANE Select	ENSP00000239243.5:n.-54C=
ENST00000239243.6:c.-54C=	ENSP00000239243.5:n.-54C=
ENST00000507785.2:c.-54C=	ENSP00000427425.1:n.-54C=
NM_002449.4:c.-54C=	NP_002440.2:n.-54C=
NM_001363626.1:c.-54C=	NP_001350555.1:n.-54C=
NM_002449.5:c.-54C= MANE Select	NP_002440.2:n.-54C=
NM_001363626.2:c.-54C=	NP_001350555.1:n.-54C=