Canonical Allele Identifier: CA247515311

Gene: KL

Linked Data

• dbSNP Id: rs775340066
• MyVariant Identifiers: chr13:g.33610066_33610067del (hg19) ; chr13:g.33035929_33035930del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.33035930_33035931del , CM000675.2:g.33035930_33035931del	GRCh38
NC_000013.10:g.33610067_33610068del , CM000675.1:g.33610067_33610068del	GRCh37
NC_000013.9:g.32508067_32508068del	NCBI36
NG_011485.1:g.24497_24498del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380099.4:c.820-17837_820-17836del MANE Select	ENSP00000369442.3:n.820-17837_820-17836del
ENST00000380099.3:c.820-17837_820-17836del	ENSP00000369442.3:n.820-17837_820-17836del
ENST00000487852.1:n.828-17837_828-17836del
NM_004795.3:c.820-17837_820-17836del	NP_004786.2:n.820-17837_820-17836del
XM_006719895.1:c.-102-17837_-102-17836del	XP_006719958.1:n.-102-17837_-102-17836del
XM_006719895.2:c.-102-17837_-102-17836del	XP_006719958.1:n.-102-17837_-102-17836del
NM_004795.4:c.820-17837_820-17836del MANE Select	NP_004786.2:n.820-17837_820-17836del