Canonical Allele Identifier: CA2083142729
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33035955_33035959delinsTTTTA , CM000675.2:g.33035955_33035959delinsTTTTA GRCh38
NC_000013.10:g.33610092_33610096delinsTTTTA , CM000675.1:g.33610092_33610096delinsTTTTA GRCh37
NC_000013.9:g.32508092_32508096delinsTTTTA NCBI36
NG_011485.1:g.24522_24526delinsTTTTA

Transcript Alleles

HGVS Amino-acid change
ENST00000380099.4:c.820-17812_820-17808delinsTTTTA MANE Select ENSP00000369442.3:n.820-17812_820-17808de...
ENST00000380099.3:c.820-17812_820-17808delinsTTTTA ENSP00000369442.3:n.820-17812_820-17808de...
ENST00000487852.1:n.828-17812_828-17808delinsTTTTA
NM_004795.3:c.820-17812_820-17808delinsTTTTA NP_004786.2:n.820-17812_820-17808delinsTT...
XM_006719895.1:c.-102-17812_-102-17808delinsTTTTA XP_006719958.1:n.-102-17812_-102-17808del...
XM_006719895.2:c.-102-17812_-102-17808delinsTTTTA XP_006719958.1:n.-102-17812_-102-17808del...
NM_004795.4:c.820-17812_820-17808delinsTTTTA MANE Select NP_004786.2:n.820-17812_820-17808delinsTT...