Canonical Allele Identifier: CA2798746675
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33036515_33036520del , CM000675.2:g.33036515_33036520del GRCh38
NC_000013.10:g.33610652_33610657del , CM000675.1:g.33610652_33610657del GRCh37
NC_000013.9:g.32508652_32508657del NCBI36
NG_011485.1:g.25082_25087del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.820-17252_820-17247del MANE Select ENSP00000369442.3:n.820-17252_820-17247del
ENST00000380099.3:c.820-17252_820-17247del ENSP00000369442.3:n.820-17252_820-17247del
ENST00000487852.1:n.828-17252_828-17247del
NM_004795.3:c.820-17252_820-17247del NP_004786.2:n.820-17252_820-17247del
XM_006719895.1:c.-102-17252_-102-17247del XP_006719958.1:n.-102-17252_-102-17247del
XM_006719895.2:c.-102-17252_-102-17247del XP_006719958.1:n.-102-17252_-102-17247del
NM_004795.4:c.820-17252_820-17247del MANE Select NP_004786.2:n.820-17252_820-17247del