Canonical Allele Identifier: CA2083133647
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33024612G= , CM000675.2:g.33024612G= GRCh38
NC_000013.10:g.33598750G= , CM000675.1:g.33598750G= GRCh37
NC_000013.9:g.32496750G= NCBI36
NG_011485.1:g.13180G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.819+7353G= MANE Select ENSP00000369442.3:n.819+7353G=
ENST00000380099.3:c.819+7353G= ENSP00000369442.3:n.819+7353G=
ENST00000487852.1:n.827+7353G=
NM_004795.3:c.819+7353G= NP_004786.2:n.819+7353G=
XM_006719895.1:c.-103+8299G= XP_006719958.1:n.-103+8299G=
XM_006719895.2:c.-103+8299G= XP_006719958.1:n.-103+8299G=
NM_004795.4:c.819+7353G= MANE Select NP_004786.2:n.819+7353G=