Canonical Allele Identifier: CA1602356144
Gene: MSX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174729306C= , CM000667.2:g.174729306C= GRCh38
NC_000005.9:g.174156309C= , CM000667.1:g.174156309C= GRCh37
NC_000005.8:g.174088915C= NCBI36
NG_008124.1:g.9735C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.527C= MANE Select ENSP00000239243.5:p.Ser176=
ENST00000239243.6:c.527C= ENSP00000239243.5:p.Ser176=
ENST00000507785.2:c.*151C= ENSP00000427425.1:n.*151C=
NM_002449.4:c.527C= NP_002440.2:p.Ser176=
NM_001363626.1:c.*151C= NP_001350555.1:n.*151C=
NM_002449.5:c.527C= MANE Select NP_002440.2:p.Ser176=
NM_001363626.2:c.*151C= NP_001350555.1:n.*151C=