Canonical Allele Identifier: CA2083133715
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33054018A= , CM000675.2:g.33054018A= GRCh38
NC_000013.10:g.33628155A= , CM000675.1:g.33628155A= GRCh37
NC_000013.9:g.32526155A= NCBI36
NG_011485.1:g.42585A=

Transcript Alleles

HGVS Amino-acid change
ENST00000380099.4:c.1071A= MANE Select ENSP00000369442.3:p.Lys357=
ENST00000380099.3:c.1071A= ENSP00000369442.3:p.Lys357=
ENST00000487852.1:n.1079A=
NM_004795.3:c.1071A= NP_004786.2:p.Lys357=
XM_006719895.1:c.150A= XP_006719958.1:p.Lys50=
XM_006719895.2:c.150A= XP_006719958.1:p.Lys50=
NM_004795.4:c.1071A= MANE Select NP_004786.2:p.Lys357=