Canonical Allele Identifier: CA2083135763
Gene: KL HGNC NCBI

Linked Data

dbSNP Id: rs1319741156

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33055392A>G , CM000675.2:g.33055392A>G GRCh38
NC_000013.10:g.33629529A>G , CM000675.1:g.33629529A>G GRCh37
NC_000013.9:g.32527529A>G NCBI36
NG_011485.1:g.43959A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.1599+77A>G MANE Select ENSP00000369442.3:n.1599+77A>G
ENST00000380099.3:c.1599+77A>G ENSP00000369442.3:n.1599+77A>G
ENST00000487852.1:n.1657+27A>G
NM_004795.3:c.1599+77A>G NP_004786.2:n.1599+77A>G
XM_006719895.1:c.678+77A>G XP_006719958.1:n.678+77A>G
XM_006719895.2:c.678+77A>G XP_006719958.1:n.678+77A>G
NM_004795.4:c.1599+77A>G MANE Select NP_004786.2:n.1599+77A>G