Canonical Allele Identifier: CA2083143073
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33036391_33036392delinsCA , CM000675.2:g.33036391_33036392delinsCA GRCh38
NC_000013.10:g.33610528_33610529delinsCA , CM000675.1:g.33610528_33610529delinsCA GRCh37
NC_000013.9:g.32508528_32508529delinsCA NCBI36
NG_011485.1:g.24958_24959delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.820-17376_820-17375delinsCA MANE Select ENSP00000369442.3:n.820-17376_820-17375delinsCA
ENST00000380099.3:c.820-17376_820-17375delinsCA ENSP00000369442.3:n.820-17376_820-17375delinsCA
ENST00000487852.1:n.828-17376_828-17375delinsCA
NM_004795.3:c.820-17376_820-17375delinsCA NP_004786.2:n.820-17376_820-17375delinsCA
XM_006719895.1:c.-102-17376_-102-17375delinsCA XP_006719958.1:n.-102-17376_-102-17375delinsCA
XM_006719895.2:c.-102-17376_-102-17375delinsCA XP_006719958.1:n.-102-17376_-102-17375delinsCA
NM_004795.4:c.820-17376_820-17375delinsCA MANE Select NP_004786.2:n.820-17376_820-17375delinsCA