Canonical Allele Identifier: CA609106289
Gene: KL HGNC NCBI

Linked Data

dbSNP Id: rs1235135609

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33036028_33036034del , CM000675.2:g.33036028_33036034del GRCh38
NC_000013.10:g.33610165_33610171del , CM000675.1:g.33610165_33610171del GRCh37
NC_000013.9:g.32508165_32508171del NCBI36
NG_011485.1:g.24595_24601del

Transcript Alleles

HGVS Amino-acid change
ENST00000380099.4:c.820-17739_820-17733del MANE Select ENSP00000369442.3:n.820-17739_820-17733de...
ENST00000380099.3:c.820-17739_820-17733del ENSP00000369442.3:n.820-17739_820-17733de...
ENST00000487852.1:n.828-17739_828-17733del
NM_004795.3:c.820-17739_820-17733del NP_004786.2:n.820-17739_820-17733del
XM_006719895.1:c.-102-17739_-102-17733del XP_006719958.1:n.-102-17739_-102-17733del...
XM_006719895.2:c.-102-17739_-102-17733del XP_006719958.1:n.-102-17739_-102-17733del...
NM_004795.4:c.820-17739_820-17733del MANE Select NP_004786.2:n.820-17739_820-17733del