Canonical Allele Identifier: CA2083133517
Gene: KL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33024507T= , CM000675.2:g.33024507T= GRCh38
NC_000013.10:g.33598645T= , CM000675.1:g.33598645T= GRCh37
NC_000013.9:g.32496645T= NCBI36
NG_011485.1:g.13075T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.819+7248T= MANE Select ENSP00000369442.3:n.819+7248T=
ENST00000380099.3:c.819+7248T= ENSP00000369442.3:n.819+7248T=
ENST00000487852.1:n.827+7248T=
NM_004795.3:c.819+7248T= NP_004786.2:n.819+7248T=
XM_006719895.1:c.-103+8194T= XP_006719958.1:n.-103+8194T=
XM_006719895.2:c.-103+8194T= XP_006719958.1:n.-103+8194T=
NM_004795.4:c.819+7248T= MANE Select NP_004786.2:n.819+7248T=
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