Canonical Allele Identifier: CA2083135794
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33055413_33055420delinsTTCTTTGA , CM000675.2:g.33055413_33055420delinsTTCTTTGA GRCh38
NC_000013.10:g.33629550_33629557delinsTTCTTTGA , CM000675.1:g.33629550_33629557delinsTTCTTTGA GRCh37
NC_000013.9:g.32527550_32527557delinsTTCTTTGA NCBI36
NG_011485.1:g.43980_43987delinsTTCTTTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.1599+98_1599+105delinsTTCTTTGA MANE Select ENSP00000369442.3:n.1599+98_1599+105delinsTTCTTTGA
ENST00000380099.3:c.1599+98_1599+105delinsTTCTTTGA ENSP00000369442.3:n.1599+98_1599+105delinsTTCTTTGA
ENST00000487852.1:n.1657+48_1657+55delinsTTCTTTGA
NM_004795.3:c.1599+98_1599+105delinsTTCTTTGA NP_004786.2:n.1599+98_1599+105delinsTTCTTTGA
XM_006719895.1:c.678+98_678+105delinsTTCTTTGA XP_006719958.1:n.678+98_678+105delinsTTCTTTGA
XM_006719895.2:c.678+98_678+105delinsTTCTTTGA XP_006719958.1:n.678+98_678+105delinsTTCTTTGA
NM_004795.4:c.1599+98_1599+105delinsTTCTTTGA MANE Select NP_004786.2:n.1599+98_1599+105delinsTTCTTTGA