Canonical Allele Identifier: CA2083135447
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33055184C= , CM000675.2:g.33055184C= GRCh38
NC_000013.10:g.33629321C= , CM000675.1:g.33629321C= GRCh37
NC_000013.9:g.32527321C= NCBI36
NG_011485.1:g.43751C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.1468C= MANE Select ENSP00000369442.3:p.Pro490=
ENST00000380099.3:c.1468C= ENSP00000369442.3:p.Pro490=
ENST00000487852.1:n.1476C=
NM_004795.3:c.1468C= NP_004786.2:p.Pro490=
XM_006719895.1:c.547C= XP_006719958.1:p.Pro183=
XM_006719895.2:c.547C= XP_006719958.1:p.Pro183=
NM_004795.4:c.1468C= MANE Select NP_004786.2:p.Pro490=