Canonical Allele Identifier: CA2083142708
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33035928_33035930delinsATC , CM000675.2:g.33035928_33035930delinsATC GRCh38
NC_000013.10:g.33610065_33610067delinsATC , CM000675.1:g.33610065_33610067delinsATC GRCh37
NC_000013.9:g.32508065_32508067delinsATC NCBI36
NG_011485.1:g.24495_24497delinsATC

Transcript Alleles

HGVS Amino-acid change
ENST00000380099.4:c.820-17839_820-17837delinsATC MANE Select ENSP00000369442.3:n.820-17839_820-17837de...
ENST00000380099.3:c.820-17839_820-17837delinsATC ENSP00000369442.3:n.820-17839_820-17837de...
ENST00000487852.1:n.828-17839_828-17837delinsATC
NM_004795.3:c.820-17839_820-17837delinsATC NP_004786.2:n.820-17839_820-17837delinsAT...
XM_006719895.1:c.-102-17839_-102-17837delinsATC XP_006719958.1:n.-102-17839_-102-17837del...
XM_006719895.2:c.-102-17839_-102-17837delinsATC XP_006719958.1:n.-102-17839_-102-17837del...
NM_004795.4:c.820-17839_820-17837delinsATC MANE Select NP_004786.2:n.820-17839_820-17837delinsAT...