Canonical Allele Identifier: CA2083133847
Gene: KL HGNC NCBI

Linked Data

dbSNP Id: rs1870705245

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33024799dup , CM000675.2:g.33024799dup GRCh38
NC_000013.10:g.33598937dup , CM000675.1:g.33598937dup GRCh37
NC_000013.9:g.32496937dup NCBI36
NG_011485.1:g.13367dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.819+7540dup MANE Select ENSP00000369442.3:n.819+7540dup
ENST00000380099.3:c.819+7540dup ENSP00000369442.3:n.819+7540dup
ENST00000487852.1:n.827+7540dup
NM_004795.3:c.819+7540dup NP_004786.2:n.819+7540dup
XM_006719895.1:c.-103+8486dup XP_006719958.1:n.-103+8486dup
XM_006719895.2:c.-103+8486dup XP_006719958.1:n.-103+8486dup
NM_004795.4:c.819+7540dup MANE Select NP_004786.2:n.819+7540dup