Canonical Allele Identifier: CA2083142746
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33035975_33036002delinsATAAGCCCTTTATTGTCACCTACTTTGG , CM000675.2:g.33035975_33036002delinsATAAGCCCTTTATTGTCACCTACTTTGG GRCh38
NC_000013.10:g.33610112_33610139delinsATAAGCCCTTTATTGTCACCTACTTTGG , CM000675.1:g.33610112_33610139delinsATAAGCCCTTTATTGTCACCTACTTTGG GRCh37
NC_000013.9:g.32508112_32508139delinsATAAGCCCTTTATTGTCACCTACTTTGG NCBI36
NG_011485.1:g.24542_24569delinsATAAGCCCTTTATTGTCACCTACTTTGG

Transcript Alleles

HGVS Amino-acid change
ENST00000380099.4:c.820-17792_820-17765delinsATAAGCCCTTTATTGTCACCTACTTTGG MANE Select ENSP00000369442.3:n.820-17792_820-17765de...
ENST00000380099.3:c.820-17792_820-17765delinsATAAGCCCTTTATTGTCACCTACTTTGG ENSP00000369442.3:n.820-17792_820-17765de...
ENST00000487852.1:n.828-17792_828-17765delinsATAAGCCCTTTATTGTCACCTACTTTGG
NM_004795.3:c.820-17792_820-17765delinsATAAGCCCTTTATTGTCACCTACTTTGG NP_004786.2:n.820-17792_820-17765delinsAT...
XM_006719895.1:c.-102-17792_-102-17765delinsATAAGCCCTTTATTGTCACCTACTTTGG XP_006719958.1:n.-102-17792_-102-17765del...
XM_006719895.2:c.-102-17792_-102-17765delinsATAAGCCCTTTATTGTCACCTACTTTGG XP_006719958.1:n.-102-17792_-102-17765del...
NM_004795.4:c.820-17792_820-17765delinsATAAGCCCTTTATTGTCACCTACTTTGG MANE Select NP_004786.2:n.820-17792_820-17765delinsAT...