Canonical Allele Identifier: CA2173247684

Linked Data

dbSNP Id: rs2085646536

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43599443del , CM000677.2:g.43599443del GRCh38
NC_000015.9:g.43891641del , CM000677.1:g.43891641del GRCh37
NC_000015.8:g.41678933del NCBI36
NG_011636.1:g.24360del

Transcript Alleles

HGVS Amino-acid Change
ENST00000411560.1:n.52del (CKMT1B)
ENST00000450892.6:c.*231del (STRC) ENSP00000401513.2:n.*231del
XM_011521277.1:c.*231del (STRC) XP_011519579.1:n.*231del
XM_011521278.1:c.*231del (STRC) XP_011519580.1:n.*231del
XM_011521279.1:c.*231del (STRC) XP_011519581.1:n.*231del