Canonical Allele Identifier: CA2628140791

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43599449_43599450del , CM000677.2:g.43599449_43599450del GRCh38
NC_000015.9:g.43891647_43891648del , CM000677.1:g.43891647_43891648del GRCh37
NC_000015.8:g.41678939_41678940del NCBI36
NG_011636.1:g.24351_24352del

Transcript Alleles

HGVS Amino-acid Change
ENST00000411560.1:n.58_59del (CKMT1B)
ENST00000450892.6:c.*222_*223del (STRC) ENSP00000401513.2:n.*222_*223del
XM_011521277.1:c.*222_*223del (STRC) XP_011519579.1:n.*222_*223del
XM_011521278.1:c.*222_*223del (STRC) XP_011519580.1:n.*222_*223del
XM_011521279.1:c.*222_*223del (STRC) XP_011519581.1:n.*222_*223del