Canonical Allele Identifier: CA2083142800
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33036060_33036061delinsCA , CM000675.2:g.33036060_33036061delinsCA GRCh38
NC_000013.10:g.33610197_33610198delinsCA , CM000675.1:g.33610197_33610198delinsCA GRCh37
NC_000013.9:g.32508197_32508198delinsCA NCBI36
NG_011485.1:g.24627_24628delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000380099.4:c.820-17707_820-17706delinsCA MANE Select ENSP00000369442.3:n.820-17707_820-17706de...
ENST00000380099.3:c.820-17707_820-17706delinsCA ENSP00000369442.3:n.820-17707_820-17706de...
ENST00000487852.1:n.828-17707_828-17706delinsCA
NM_004795.3:c.820-17707_820-17706delinsCA NP_004786.2:n.820-17707_820-17706delinsCA...
XM_006719895.1:c.-102-17707_-102-17706delinsCA XP_006719958.1:n.-102-17707_-102-17706del...
XM_006719895.2:c.-102-17707_-102-17706delinsCA XP_006719958.1:n.-102-17707_-102-17706del...
NM_004795.4:c.820-17707_820-17706delinsCA MANE Select NP_004786.2:n.820-17707_820-17706delinsCA...