Canonical Allele Identifier: CA2841554166

Gene: KL

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.33035736_33035737insAG , CM000675.2:g.33035736_33035737insAG	GRCh38
NC_000013.10:g.33609873_33609874insAG , CM000675.1:g.33609873_33609874insAG	GRCh37
NC_000013.9:g.32507873_32507874insAG	NCBI36
NG_011485.1:g.24303_24304insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380099.4:c.820-18031_820-18030insAG MANE Select	ENSP00000369442.3:n.820-18031_820-18030insAG
ENST00000380099.3:c.820-18031_820-18030insAG	ENSP00000369442.3:n.820-18031_820-18030insAG
ENST00000487852.1:n.828-18031_828-18030insAG
NM_004795.3:c.820-18031_820-18030insAG	NP_004786.2:n.820-18031_820-18030insAG
XM_006719895.1:c.-102-18031_-102-18030insAG	XP_006719958.1:n.-102-18031_-102-18030insAG
XM_006719895.2:c.-102-18031_-102-18030insAG	XP_006719958.1:n.-102-18031_-102-18030insAG
NM_004795.4:c.820-18031_820-18030insAG MANE Select	NP_004786.2:n.820-18031_820-18030insAG