Canonical Allele Identifier: CA2545960216
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33024804G>T , CM000675.2:g.33024804G>T GRCh38
NC_000013.10:g.33598942G>T , CM000675.1:g.33598942G>T GRCh37
NC_000013.9:g.32496942G>T NCBI36
NG_011485.1:g.13372G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000380099.4:c.819+7545G>T MANE Select ENSP00000369442.3:n.819+7545G>T
ENST00000380099.3:c.819+7545G>T ENSP00000369442.3:n.819+7545G>T
ENST00000487852.1:n.827+7545G>T
NM_004795.3:c.819+7545G>T NP_004786.2:n.819+7545G>T
XM_006719895.1:c.-103+8491G>T XP_006719958.1:n.-103+8491G>T
XM_006719895.2:c.-103+8491G>T XP_006719958.1:n.-103+8491G>T
NM_004795.4:c.819+7545G>T MANE Select NP_004786.2:n.819+7545G>T