Canonical Allele Identifier: CA387789991
Gene: KL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33053812A>T , CM000675.2:g.33053812A>T GRCh38
NC_000013.10:g.33627949A>T , CM000675.1:g.33627949A>T GRCh37
NC_000013.9:g.32525949A>T NCBI36
NG_011485.1:g.42379A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.865A>T MANE Select ENSP00000369442.3:p.Thr289Ser
ENST00000380099.3:c.865A>T ENSP00000369442.3:p.Thr289Ser
ENST00000487852.1:n.873A>T
NM_004795.3:c.865A>T NP_004786.2:p.Thr289Ser
XM_006719895.1:c.-57A>T XP_006719958.1:n.-57A>T
XM_006719895.2:c.-57A>T XP_006719958.1:n.-57A>T
NM_004795.4:c.865A>T MANE Select NP_004786.2:p.Thr289Ser