Canonical Allele Identifier: CA2695233477

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949915_43949919delinsCGAGGCAT , CM000685.2:g.43949915_43949919delinsCGAGGCAT GRCh38
NC_000023.10:g.43809161_43809165delinsCGAGGCAT , CM000685.1:g.43809161_43809165delinsCGAGGCAT GRCh37
NC_000023.9:g.43694105_43694109delinsCGAGGCAT NCBI36
NG_009832.1:g.28757_28761delinsATGCCTCG

Transcript Alleles

HGVS Amino-acid change
ENST00000642620.1:c.282_286delinsATGCCTCG (NDP) MANE Select ENSP00000495972.1:p.His94_Cys96delinsGlnC...
ENST00000647044.1:c.282_286delinsATGCCTCG (NDP) ENSP00000495811.1:p.His94_Cys96delinsGlnC...
ENST00000378062.5:c.282_286delinsATGCCTCG (NDP) ENSP00000367301.5:p.His94_Cys96delinsGlnC...
ENST00000470584.1:n.326_330delinsATGCCTCG (NDP)
NM_000266.3:c.282_286delinsATGCCTCG (NDP) NP_000257.1:p.His94_Cys96delinsGlnCysLeuG...
NR_046631.1:n.184_188delinsCGAGGCAT (NDP-AS1)
NM_000266.4:c.282_286delinsATGCCTCG (NDP) MANE Select NP_000257.1:p.His94_Cys96delinsGlnCysLeuG...