Canonical Allele Identifier: CA2083142790
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33036042A= , CM000675.2:g.33036042A= GRCh38
NC_000013.10:g.33610179A= , CM000675.1:g.33610179A= GRCh37
NC_000013.9:g.32508179A= NCBI36
NG_011485.1:g.24609A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.820-17725A= MANE Select ENSP00000369442.3:n.820-17725A=
ENST00000380099.3:c.820-17725A= ENSP00000369442.3:n.820-17725A=
ENST00000487852.1:n.828-17725A=
NM_004795.3:c.820-17725A= NP_004786.2:n.820-17725A=
XM_006719895.1:c.-102-17725A= XP_006719958.1:n.-102-17725A=
XM_006719895.2:c.-102-17725A= XP_006719958.1:n.-102-17725A=
NM_004795.4:c.820-17725A= MANE Select NP_004786.2:n.820-17725A=