Canonical Allele Identifier: CA483442286
Gene: KL HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.33629359G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33055222G>A , CM000675.2:g.33055222G>A GRCh38
NC_000013.10:g.33629359G>A , CM000675.1:g.33629359G>A GRCh37
NC_000013.9:g.32527359G>A NCBI36
NG_011485.1:g.43789G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.1506G>A MANE Select ENSP00000369442.3:p.Glu502=
ENST00000380099.3:c.1506G>A ENSP00000369442.3:p.Glu502=
ENST00000487852.1:n.1514G>A
NM_004795.3:c.1506G>A NP_004786.2:p.Glu502=
XM_006719895.1:c.585G>A XP_006719958.1:p.Glu195=
XM_006719895.2:c.585G>A XP_006719958.1:p.Glu195=
NM_004795.4:c.1506G>A MANE Select NP_004786.2:p.Glu502=
Search 100 bp 5'
Search 100 bp 3'