Canonical Allele Identifier: CA2083142815
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33036076C= , CM000675.2:g.33036076C= GRCh38
NC_000013.10:g.33610213C= , CM000675.1:g.33610213C= GRCh37
NC_000013.9:g.32508213C= NCBI36
NG_011485.1:g.24643C=

Transcript Alleles

HGVS Amino-acid change
ENST00000380099.4:c.820-17691C= MANE Select ENSP00000369442.3:n.820-17691C=
ENST00000380099.3:c.820-17691C= ENSP00000369442.3:n.820-17691C=
ENST00000487852.1:n.828-17691C=
NM_004795.3:c.820-17691C= NP_004786.2:n.820-17691C=
XM_006719895.1:c.-102-17691C= XP_006719958.1:n.-102-17691C=
XM_006719895.2:c.-102-17691C= XP_006719958.1:n.-102-17691C=
NM_004795.4:c.820-17691C= MANE Select NP_004786.2:n.820-17691C=