Canonical Allele Identifier: CA2083143179
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33036556_33036557delinsTC , CM000675.2:g.33036556_33036557delinsTC GRCh38
NC_000013.10:g.33610693_33610694delinsTC , CM000675.1:g.33610693_33610694delinsTC GRCh37
NC_000013.9:g.32508693_32508694delinsTC NCBI36
NG_011485.1:g.25123_25124delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.820-17211_820-17210delinsTC MANE Select ENSP00000369442.3:n.820-17211_820-17210delinsTC
ENST00000380099.3:c.820-17211_820-17210delinsTC ENSP00000369442.3:n.820-17211_820-17210delinsTC
ENST00000487852.1:n.828-17211_828-17210delinsTC
NM_004795.3:c.820-17211_820-17210delinsTC NP_004786.2:n.820-17211_820-17210delinsTC
XM_006719895.1:c.-102-17211_-102-17210delinsTC XP_006719958.1:n.-102-17211_-102-17210delinsTC
XM_006719895.2:c.-102-17211_-102-17210delinsTC XP_006719958.1:n.-102-17211_-102-17210delinsTC
NM_004795.4:c.820-17211_820-17210delinsTC MANE Select NP_004786.2:n.820-17211_820-17210delinsTC