Canonical Allele Identifier: CA2083135843
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33055448_33055449delinsTA , CM000675.2:g.33055448_33055449delinsTA GRCh38
NC_000013.10:g.33629585_33629586delinsTA , CM000675.1:g.33629585_33629586delinsTA GRCh37
NC_000013.9:g.32527585_32527586delinsTA NCBI36
NG_011485.1:g.44015_44016delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.1599+133_1599+134delinsTA MANE Select ENSP00000369442.3:n.1599+133_1599+134delinsTA
ENST00000380099.3:c.1599+133_1599+134delinsTA ENSP00000369442.3:n.1599+133_1599+134delinsTA
ENST00000487852.1:n.1657+83_1657+84delinsTA
NM_004795.3:c.1599+133_1599+134delinsTA NP_004786.2:n.1599+133_1599+134delinsTA
XM_006719895.1:c.678+133_678+134delinsTA XP_006719958.1:n.678+133_678+134delinsTA
XM_006719895.2:c.678+133_678+134delinsTA XP_006719958.1:n.678+133_678+134delinsTA
NM_004795.4:c.1599+133_1599+134delinsTA MANE Select NP_004786.2:n.1599+133_1599+134delinsTA