Canonical Allele Identifier: CA2083143150
Gene: KL HGNC NCBI

Linked Data

dbSNP Id: rs1871151826

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33036523A>T , CM000675.2:g.33036523A>T GRCh38
NC_000013.10:g.33610660A>T , CM000675.1:g.33610660A>T GRCh37
NC_000013.9:g.32508660A>T NCBI36
NG_011485.1:g.25090A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.820-17244A>T MANE Select ENSP00000369442.3:n.820-17244A>T
ENST00000380099.3:c.820-17244A>T ENSP00000369442.3:n.820-17244A>T
ENST00000487852.1:n.828-17244A>T
NM_004795.3:c.820-17244A>T NP_004786.2:n.820-17244A>T
XM_006719895.1:c.-102-17244A>T XP_006719958.1:n.-102-17244A>T
XM_006719895.2:c.-102-17244A>T XP_006719958.1:n.-102-17244A>T
NM_004795.4:c.820-17244A>T MANE Select NP_004786.2:n.820-17244A>T