Canonical Allele Identifier: CA247515388
Gene: KL HGNC NCBI

Linked Data

dbSNP Id: rs369374824

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33036085G>A , CM000675.2:g.33036085G>A GRCh38
NC_000013.10:g.33610222G>A , CM000675.1:g.33610222G>A GRCh37
NC_000013.9:g.32508222G>A NCBI36
NG_011485.1:g.24652G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000380099.4:c.820-17682G>A MANE Select ENSP00000369442.3:n.820-17682G>A
ENST00000380099.3:c.820-17682G>A ENSP00000369442.3:n.820-17682G>A
ENST00000487852.1:n.828-17682G>A
NM_004795.3:c.820-17682G>A NP_004786.2:n.820-17682G>A
XM_006719895.1:c.-102-17682G>A XP_006719958.1:n.-102-17682G>A
XM_006719895.2:c.-102-17682G>A XP_006719958.1:n.-102-17682G>A
NM_004795.4:c.820-17682G>A MANE Select NP_004786.2:n.820-17682G>A