Canonical Allele Identifier: CA2173247683

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43599440_43599441delinsAG , CM000677.2:g.43599440_43599441delinsAG GRCh38
NC_000015.9:g.43891638_43891639delinsAG , CM000677.1:g.43891638_43891639delinsAG GRCh37
NC_000015.8:g.41678930_41678931delinsAG NCBI36
NG_011636.1:g.24360_24361delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000411560.1:n.49_50delinsAG (CKMT1B)
ENST00000450892.6:c.*231_*232delinsCT (STRC) ENSP00000401513.2:n.*231_*232delinsCT
XM_011521277.1:c.*231_*232delinsCT (STRC) XP_011519579.1:n.*231_*232delinsCT
XM_011521278.1:c.*231_*232delinsCT (STRC) XP_011519580.1:n.*231_*232delinsCT
XM_011521279.1:c.*231_*232delinsCT (STRC) XP_011519581.1:n.*231_*232delinsCT