Canonical Allele Identifier: CA2727833497
Gene: KL HGNC NCBI

Linked Data

dbSNP Id: rs71196504

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33036422_33036425del , CM000675.2:g.33036422_33036425del GRCh38
NC_000013.10:g.33610559_33610562del , CM000675.1:g.33610559_33610562del GRCh37
NC_000013.9:g.32508559_32508562del NCBI36
NG_011485.1:g.24989_24992del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.820-17345_820-17342del MANE Select ENSP00000369442.3:n.820-17345_820-17342del
ENST00000380099.3:c.820-17345_820-17342del ENSP00000369442.3:n.820-17345_820-17342del
ENST00000487852.1:n.828-17345_828-17342del
NM_004795.3:c.820-17345_820-17342del NP_004786.2:n.820-17345_820-17342del
XM_006719895.1:c.-102-17345_-102-17342del XP_006719958.1:n.-102-17345_-102-17342del
XM_006719895.2:c.-102-17345_-102-17342del XP_006719958.1:n.-102-17345_-102-17342del
NM_004795.4:c.820-17345_820-17342del MANE Select NP_004786.2:n.820-17345_820-17342del