Canonical Allele Identifier: CA2083142665

Gene: KL

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.33035893_33035894delinsAT , CM000675.2:g.33035893_33035894delinsAT	GRCh38
NC_000013.10:g.33610030_33610031delinsAT , CM000675.1:g.33610030_33610031delinsAT	GRCh37
NC_000013.9:g.32508030_32508031delinsAT	NCBI36
NG_011485.1:g.24460_24461delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380099.4:c.820-17874_820-17873delinsAT MANE Select	ENSP00000369442.3:n.820-17874_820-17873delinsAT
ENST00000380099.3:c.820-17874_820-17873delinsAT	ENSP00000369442.3:n.820-17874_820-17873delinsAT
ENST00000487852.1:n.828-17874_828-17873delinsAT
NM_004795.3:c.820-17874_820-17873delinsAT	NP_004786.2:n.820-17874_820-17873delinsAT
XM_006719895.1:c.-102-17874_-102-17873delinsAT	XP_006719958.1:n.-102-17874_-102-17873delinsAT
XM_006719895.2:c.-102-17874_-102-17873delinsAT	XP_006719958.1:n.-102-17874_-102-17873delinsAT
NM_004795.4:c.820-17874_820-17873delinsAT MANE Select	NP_004786.2:n.820-17874_820-17873delinsAT