Canonical Allele Identifier: CA2083142808
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33036074A= , CM000675.2:g.33036074A= GRCh38
NC_000013.10:g.33610211A= , CM000675.1:g.33610211A= GRCh37
NC_000013.9:g.32508211A= NCBI36
NG_011485.1:g.24641A=

Transcript Alleles

HGVS Amino-acid change
ENST00000380099.4:c.820-17693A= MANE Select ENSP00000369442.3:n.820-17693A=
ENST00000380099.3:c.820-17693A= ENSP00000369442.3:n.820-17693A=
ENST00000487852.1:n.828-17693A=
NM_004795.3:c.820-17693A= NP_004786.2:n.820-17693A=
XM_006719895.1:c.-102-17693A= XP_006719958.1:n.-102-17693A=
XM_006719895.2:c.-102-17693A= XP_006719958.1:n.-102-17693A=
NM_004795.4:c.820-17693A= MANE Select NP_004786.2:n.820-17693A=