Canonical Allele Identifier: CA1602344944
Gene: MSX2 HGNC NCBI

Linked Data

dbSNP Id: rs1760728552
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724582del , CM000667.2:g.174724582del GRCh38
NC_000005.9:g.174151585del , CM000667.1:g.174151585del GRCh37
NC_000005.8:g.174084191del NCBI36
NG_008124.1:g.5011del

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.-78del MANE Select ENSP00000239243.5:n.-78del
ENST00000239243.6:c.-78del ENSP00000239243.5:n.-78del
NM_002449.4:c.-78del NP_002440.2:n.-78del
NM_001363626.1:c.-78del NP_001350555.1:n.-78del
NM_002449.5:c.-78del MANE Select NP_002440.2:n.-78del
NM_001363626.2:c.-78del NP_001350555.1:n.-78del
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