Canonical Allele Identifier: CA2083143169
Gene: KL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33036544C= , CM000675.2:g.33036544C= GRCh38
NC_000013.10:g.33610681C= , CM000675.1:g.33610681C= GRCh37
NC_000013.9:g.32508681C= NCBI36
NG_011485.1:g.25111C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.820-17223C= MANE Select ENSP00000369442.3:n.820-17223C=
ENST00000380099.3:c.820-17223C= ENSP00000369442.3:n.820-17223C=
ENST00000487852.1:n.828-17223C=
NM_004795.3:c.820-17223C= NP_004786.2:n.820-17223C=
XM_006719895.1:c.-102-17223C= XP_006719958.1:n.-102-17223C=
XM_006719895.2:c.-102-17223C= XP_006719958.1:n.-102-17223C=
NM_004795.4:c.820-17223C= MANE Select NP_004786.2:n.820-17223C=
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