Canonical Allele Identifier: CA247515553

Gene: KL

Linked Data

• dbSNP Id: rs781383443
• MyVariant Identifiers: chr13:g.33610537_33610538del (hg19) ; chr13:g.33036400_33036401del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.33036409_33036410del , CM000675.2:g.33036409_33036410del	GRCh38
NC_000013.10:g.33610546_33610547del , CM000675.1:g.33610546_33610547del	GRCh37
NC_000013.9:g.32508546_32508547del	NCBI36
NG_011485.1:g.24976_24977del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380099.4:c.820-17358_820-17357del MANE Select	ENSP00000369442.3:n.820-17358_820-17357del
ENST00000380099.3:c.820-17358_820-17357del	ENSP00000369442.3:n.820-17358_820-17357del
ENST00000487852.1:n.828-17358_828-17357del
NM_004795.3:c.820-17358_820-17357del	NP_004786.2:n.820-17358_820-17357del
XM_006719895.1:c.-102-17358_-102-17357del	XP_006719958.1:n.-102-17358_-102-17357del
XM_006719895.2:c.-102-17358_-102-17357del	XP_006719958.1:n.-102-17358_-102-17357del
NM_004795.4:c.820-17358_820-17357del MANE Select	NP_004786.2:n.820-17358_820-17357del