Canonical Allele Identifier: CA2083142730
Gene: KL HGNC NCBI

Linked Data

dbSNP Id: rs1871135462

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33035960_33035963del , CM000675.2:g.33035960_33035963del GRCh38
NC_000013.10:g.33610097_33610100del , CM000675.1:g.33610097_33610100del GRCh37
NC_000013.9:g.32508097_32508100del NCBI36
NG_011485.1:g.24527_24530del

Transcript Alleles

HGVS Amino-acid change
ENST00000380099.4:c.820-17807_820-17804del MANE Select ENSP00000369442.3:n.820-17807_820-17804de...
ENST00000380099.3:c.820-17807_820-17804del ENSP00000369442.3:n.820-17807_820-17804de...
ENST00000487852.1:n.828-17807_828-17804del
NM_004795.3:c.820-17807_820-17804del NP_004786.2:n.820-17807_820-17804del
XM_006719895.1:c.-102-17807_-102-17804del XP_006719958.1:n.-102-17807_-102-17804del...
XM_006719895.2:c.-102-17807_-102-17804del XP_006719958.1:n.-102-17807_-102-17804del...
NM_004795.4:c.820-17807_820-17804del MANE Select NP_004786.2:n.820-17807_820-17804del