Canonical Allele Identifier: CA2083135986

Gene: KL

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.33055592_33055594delinsCTT , CM000675.2:g.33055592_33055594delinsCTT	GRCh38
NC_000013.10:g.33629729_33629731delinsCTT , CM000675.1:g.33629729_33629731delinsCTT	GRCh37
NC_000013.9:g.32527729_32527731delinsCTT	NCBI36
NG_011485.1:g.44159_44161delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380099.4:c.1599+277_1599+279delinsCTT MANE Select	ENSP00000369442.3:n.1599+277_1599+279delinsCTT
ENST00000380099.3:c.1599+277_1599+279delinsCTT	ENSP00000369442.3:n.1599+277_1599+279delinsCTT
ENST00000487852.1:n.1657+227_1657+229delinsCTT
NM_004795.3:c.1599+277_1599+279delinsCTT	NP_004786.2:n.1599+277_1599+279delinsCTT
XM_006719895.1:c.678+277_678+279delinsCTT	XP_006719958.1:n.678+277_678+279delinsCTT
XM_006719895.2:c.678+277_678+279delinsCTT	XP_006719958.1:n.678+277_678+279delinsCTT
NM_004795.4:c.1599+277_1599+279delinsCTT MANE Select	NP_004786.2:n.1599+277_1599+279delinsCTT