Canonical Allele Identifier: CA2083133846
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33024798A= , CM000675.2:g.33024798A= GRCh38
NC_000013.10:g.33598936A= , CM000675.1:g.33598936A= GRCh37
NC_000013.9:g.32496936A= NCBI36
NG_011485.1:g.13366A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.819+7539A= MANE Select ENSP00000369442.3:n.819+7539A=
ENST00000380099.3:c.819+7539A= ENSP00000369442.3:n.819+7539A=
ENST00000487852.1:n.827+7539A=
NM_004795.3:c.819+7539A= NP_004786.2:n.819+7539A=
XM_006719895.1:c.-103+8485A= XP_006719958.1:n.-103+8485A=
XM_006719895.2:c.-103+8485A= XP_006719958.1:n.-103+8485A=
NM_004795.4:c.819+7539A= MANE Select NP_004786.2:n.819+7539A=