Canonical Allele Identifier: CA2578488479
Gene: MSX2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724618del , CM000667.2:g.174724618del GRCh38
NC_000005.9:g.174151621del , CM000667.1:g.174151621del GRCh37
NC_000005.8:g.174084227del NCBI36
NG_008124.1:g.5047del

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.-42del MANE Select ENSP00000239243.5:n.-42del
ENST00000239243.6:c.-42del ENSP00000239243.5:n.-42del
ENST00000507785.2:c.-42del ENSP00000427425.1:n.-42del
NM_002449.4:c.-42del NP_002440.2:n.-42del
NM_001363626.1:c.-42del NP_001350555.1:n.-42del
NM_002449.5:c.-42del MANE Select NP_002440.2:n.-42del
NM_001363626.2:c.-42del NP_001350555.1:n.-42del
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