Canonical Allele Identifier: CA1602347063
Gene: MSX2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174725106_174725107delinsCC , CM000667.2:g.174725106_174725107delinsCC GRCh38
NC_000005.9:g.174152109_174152110delinsCC , CM000667.1:g.174152109_174152110delinsCC GRCh37
NC_000005.8:g.174084715_174084716delinsCC NCBI36
NG_008124.1:g.5535_5536delinsCC

Transcript Alleles

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