Canonical Allele Identifier: CA2628140773

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43599430_43599431del , CM000677.2:g.43599430_43599431del GRCh38
NC_000015.9:g.43891628_43891629del , CM000677.1:g.43891628_43891629del GRCh37
NC_000015.8:g.41678920_41678921del NCBI36
NG_011636.1:g.24371_24372del

Transcript Alleles

HGVS Amino-acid Change
ENST00000411560.1:n.39_40del (CKMT1B)
ENST00000450892.6:c.*242_*243del (STRC) ENSP00000401513.2:n.*242_*243del
XM_011521277.1:c.*242_*243del (STRC) XP_011519579.1:n.*242_*243del
XM_011521278.1:c.*242_*243del (STRC) XP_011519580.1:n.*242_*243del
XM_011521279.1:c.*242_*243del (STRC) XP_011519581.1:n.*242_*243del