Canonical Allele Identifier: CA2504870545
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33035987_33035988del , CM000675.2:g.33035987_33035988del GRCh38
NC_000013.10:g.33610124_33610125del , CM000675.1:g.33610124_33610125del GRCh37
NC_000013.9:g.32508124_32508125del NCBI36
NG_011485.1:g.24554_24555del

Transcript Alleles

HGVS Amino-acid change
ENST00000380099.4:c.820-17780_820-17779del MANE Select ENSP00000369442.3:n.820-17780_820-17779de...
ENST00000380099.3:c.820-17780_820-17779del ENSP00000369442.3:n.820-17780_820-17779de...
ENST00000487852.1:n.828-17780_828-17779del
NM_004795.3:c.820-17780_820-17779del NP_004786.2:n.820-17780_820-17779del
XM_006719895.1:c.-102-17780_-102-17779del XP_006719958.1:n.-102-17780_-102-17779del...
XM_006719895.2:c.-102-17780_-102-17779del XP_006719958.1:n.-102-17780_-102-17779del...
NM_004795.4:c.820-17780_820-17779del MANE Select NP_004786.2:n.820-17780_820-17779del