Canonical Allele Identifier: CA132700929
Gene: MSX2 HGNC NCBI

Linked Data

dbSNP Id: rs386695185
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174725106_174725107delinsTT , CM000667.2:g.174725106_174725107delinsTT GRCh38
NC_000005.9:g.174152109_174152110delinsTT , CM000667.1:g.174152109_174152110delinsTT GRCh37
NC_000005.8:g.174084715_174084716delinsTT NCBI36
NG_008124.1:g.5535_5536delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.379+68_379+69delinsTT MANE Select ENSP00000239243.5:n.379+68_379+69delinsTT
ENST00000239243.6:c.379+68_379+69delinsTT ENSP00000239243.5:n.379+68_379+69delinsTT
ENST00000507785.2:c.*3+39_*3+40delinsTT ENSP00000427425.1:n.*3+39_*3+40delinsTT
NM_002449.4:c.379+68_379+69delinsTT NP_002440.2:n.379+68_379+69delinsTT
NM_001363626.1:c.*3+39_*3+40delinsTT NP_001350555.1:n.*3+39_*3+40delinsTT
NM_002449.5:c.379+68_379+69delinsTT MANE Select NP_002440.2:n.379+68_379+69delinsTT
NM_001363626.2:c.*3+39_*3+40delinsTT NP_001350555.1:n.*3+39_*3+40delinsTT
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