Canonical Allele Identifier: CA483442138
Gene: KL HGNC NCBI

Linked Data

dbSNP Id: rs1871910106
COSMIC: COSM4795132 COSM4795133
MyVariant Identifiers: chr13:g.33629305G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33055168G>A , CM000675.2:g.33055168G>A GRCh38
NC_000013.10:g.33629305G>A , CM000675.1:g.33629305G>A GRCh37
NC_000013.9:g.32527305G>A NCBI36
NG_011485.1:g.43735G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.1452G>A MANE Select ENSP00000369442.3:p.Gln484=
ENST00000380099.3:c.1452G>A ENSP00000369442.3:p.Gln484=
ENST00000487852.1:n.1460G>A
NM_004795.3:c.1452G>A NP_004786.2:p.Gln484=
XM_006719895.1:c.531G>A XP_006719958.1:p.Gln177=
XM_006719895.2:c.531G>A XP_006719958.1:p.Gln177=
NM_004795.4:c.1452G>A MANE Select NP_004786.2:p.Gln484=
Search 100 bp 5'
Search 100 bp 3'