Canonical Allele Identifier: CA2083143094
Gene: KL HGNC NCBI

Linked Data

dbSNP Id: rs1871148749

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33036410_33036411insA , CM000675.2:g.33036410_33036411insA GRCh38
NC_000013.10:g.33610547_33610548insA , CM000675.1:g.33610547_33610548insA GRCh37
NC_000013.9:g.32508547_32508548insA NCBI36
NG_011485.1:g.24977_24978insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.820-17357_820-17356insA MANE Select ENSP00000369442.3:n.820-17357_820-17356insA
ENST00000380099.3:c.820-17357_820-17356insA ENSP00000369442.3:n.820-17357_820-17356insA
ENST00000487852.1:n.828-17357_828-17356insA
NM_004795.3:c.820-17357_820-17356insA NP_004786.2:n.820-17357_820-17356insA
XM_006719895.1:c.-102-17357_-102-17356insA XP_006719958.1:n.-102-17357_-102-17356insA
XM_006719895.2:c.-102-17357_-102-17356insA XP_006719958.1:n.-102-17357_-102-17356insA
NM_004795.4:c.820-17357_820-17356insA MANE Select NP_004786.2:n.820-17357_820-17356insA