Canonical Allele Identifier: CA954749538
Gene: KL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33036426_33036433del , CM000675.2:g.33036426_33036433del GRCh38
NC_000013.10:g.33610563_33610570del , CM000675.1:g.33610563_33610570del GRCh37
NC_000013.9:g.32508563_32508570del NCBI36
NG_011485.1:g.24993_25000del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.820-17341_820-17334del MANE Select ENSP00000369442.3:n.820-17341_820-17334del
ENST00000380099.3:c.820-17341_820-17334del ENSP00000369442.3:n.820-17341_820-17334del
ENST00000487852.1:n.828-17341_828-17334del
NM_004795.3:c.820-17341_820-17334del NP_004786.2:n.820-17341_820-17334del
XM_006719895.1:c.-102-17341_-102-17334del XP_006719958.1:n.-102-17341_-102-17334del
XM_006719895.2:c.-102-17341_-102-17334del XP_006719958.1:n.-102-17341_-102-17334del
NM_004795.4:c.820-17341_820-17334del MANE Select NP_004786.2:n.820-17341_820-17334del