Canonical Allele Identifier: CA2083143079
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33036394_33036410delinsACACACCACACACACAC , CM000675.2:g.33036394_33036410delinsACACACCACACACACAC GRCh38
NC_000013.10:g.33610531_33610547delinsACACACCACACACACAC , CM000675.1:g.33610531_33610547delinsACACACCACACACACAC GRCh37
NC_000013.9:g.32508531_32508547delinsACACACCACACACACAC NCBI36
NG_011485.1:g.24961_24977delinsACACACCACACACACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.820-17373_820-17357delinsACACACCACACACACAC MANE Select ENSP00000369442.3:n.820-17373_820-17357delinsACACACCACACACACA...
ENST00000380099.3:c.820-17373_820-17357delinsACACACCACACACACAC ENSP00000369442.3:n.820-17373_820-17357delinsACACACCACACACACA...
ENST00000487852.1:n.828-17373_828-17357delinsACACACCACACACACAC
NM_004795.3:c.820-17373_820-17357delinsACACACCACACACACAC NP_004786.2:n.820-17373_820-17357delinsACACACCACACACACAC
XM_006719895.1:c.-102-17373_-102-17357delinsACACACCACACACACAC XP_006719958.1:n.-102-17373_-102-17357delinsACACACCACACACACAC...
XM_006719895.2:c.-102-17373_-102-17357delinsACACACCACACACACAC XP_006719958.1:n.-102-17373_-102-17357delinsACACACCACACACACAC...
NM_004795.4:c.820-17373_820-17357delinsACACACCACACACACAC MANE Select NP_004786.2:n.820-17373_820-17357delinsACACACCACACACACAC