Canonical Allele Identifier: CA387792785
Gene: KL HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.33629405A>C (hg19) chr13:g.33055268A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33055268A>C , CM000675.2:g.33055268A>C GRCh38
NC_000013.10:g.33629405A>C , CM000675.1:g.33629405A>C GRCh37
NC_000013.9:g.32527405A>C NCBI36
NG_011485.1:g.43835A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000380099.4:c.1552A>C MANE Select ENSP00000369442.3:p.Thr518Pro
ENST00000380099.3:c.1552A>C ENSP00000369442.3:p.Thr518Pro
ENST00000487852.1:n.1560A>C
NM_004795.3:c.1552A>C NP_004786.2:p.Thr518Pro
XM_006719895.1:c.631A>C XP_006719958.1:p.Thr211Pro
XM_006719895.2:c.631A>C XP_006719958.1:p.Thr211Pro
NM_004795.4:c.1552A>C MANE Select NP_004786.2:p.Thr518Pro
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