Canonical Allele Identifier: CA2083142748

Gene: KL

Linked Data

• dbSNP Id: rs1871136091

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.33035976_33036002del , CM000675.2:g.33035976_33036002del	GRCh38
NC_000013.10:g.33610113_33610139del , CM000675.1:g.33610113_33610139del	GRCh37
NC_000013.9:g.32508113_32508139del	NCBI36
NG_011485.1:g.24543_24569del

Transcript Alleles

HGVS	Amino-acid change
ENST00000380099.4:c.820-17791_820-17765del MANE Select	ENSP00000369442.3:n.820-17791_820-17765de...
ENST00000380099.3:c.820-17791_820-17765del	ENSP00000369442.3:n.820-17791_820-17765de...
ENST00000487852.1:n.828-17791_828-17765del
NM_004795.3:c.820-17791_820-17765del	NP_004786.2:n.820-17791_820-17765del
XM_006719895.1:c.-102-17791_-102-17765del	XP_006719958.1:n.-102-17791_-102-17765del...
XM_006719895.2:c.-102-17791_-102-17765del	XP_006719958.1:n.-102-17791_-102-17765del...
NM_004795.4:c.820-17791_820-17765del MANE Select	NP_004786.2:n.820-17791_820-17765del