Canonical Allele Identifier: CA2803948517

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43599518del , CM000677.2:g.43599518del GRCh38
NC_000015.9:g.43891716del , CM000677.1:g.43891716del GRCh37
NC_000015.8:g.41679008del NCBI36
NG_011636.1:g.24284del

Transcript Alleles

HGVS Amino-acid Change
ENST00000411560.1:n.127del (CKMT1B)
ENST00000450892.6:c.*155del (STRC) ENSP00000401513.2:n.*155del
XM_011521277.1:c.*155del (STRC) XP_011519579.1:n.*155del
XM_011521278.1:c.*155del (STRC) XP_011519580.1:n.*155del
XM_011521279.1:c.*155del (STRC) XP_011519581.1:n.*155del