Canonical Allele Identifier: CA2083135740
Gene: KL HGNC NCBI

Linked Data

dbSNP Id: rs1871920646

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33055376C>G , CM000675.2:g.33055376C>G GRCh38
NC_000013.10:g.33629513C>G , CM000675.1:g.33629513C>G GRCh37
NC_000013.9:g.32527513C>G NCBI36
NG_011485.1:g.43943C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.1599+61C>G MANE Select ENSP00000369442.3:n.1599+61C>G
ENST00000380099.3:c.1599+61C>G ENSP00000369442.3:n.1599+61C>G
ENST00000487852.1:n.1657+11C>G
NM_004795.3:c.1599+61C>G NP_004786.2:n.1599+61C>G
XM_006719895.1:c.678+61C>G XP_006719958.1:n.678+61C>G
XM_006719895.2:c.678+61C>G XP_006719958.1:n.678+61C>G
NM_004795.4:c.1599+61C>G MANE Select NP_004786.2:n.1599+61C>G