Canonical Allele Identifier: CA1602344940
Gene: MSX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724581_174724582delinsCG , CM000667.2:g.174724581_174724582delinsCG GRCh38
NC_000005.9:g.174151584_174151585delinsCG , CM000667.1:g.174151584_174151585delinsCG GRCh37
NC_000005.8:g.174084190_174084191delinsCG NCBI36
NG_008124.1:g.5010_5011delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.6:c.-79_-78delinsCG ENSP00000239243.5:n.-79_-78delinsCG
NM_002449.4:c.-79_-78delinsCG NP_002440.2:n.-79_-78delinsCG
NM_001363626.1:c.-79_-78delinsCG NP_001350555.1:n.-79_-78delinsCG