Canonical Allele Identifier: CA483441859
Gene: KL HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.33628158G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33054021G>A , CM000675.2:g.33054021G>A GRCh38
NC_000013.10:g.33628158G>A , CM000675.1:g.33628158G>A GRCh37
NC_000013.9:g.32526158G>A NCBI36
NG_011485.1:g.42588G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.1074G>A MANE Select ENSP00000369442.3:p.Lys358=
ENST00000380099.3:c.1074G>A ENSP00000369442.3:p.Lys358=
ENST00000487852.1:n.1082G>A
NM_004795.3:c.1074G>A NP_004786.2:p.Lys358=
XM_006719895.1:c.153G>A XP_006719958.1:p.Lys51=
XM_006719895.2:c.153G>A XP_006719958.1:p.Lys51=
NM_004795.4:c.1074G>A MANE Select NP_004786.2:p.Lys358=
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