Canonical Allele Identifier: CA2739436841
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33055319A>T , CM000675.2:g.33055319A>T GRCh38
NC_000013.10:g.33629456A>T , CM000675.1:g.33629456A>T GRCh37
NC_000013.9:g.32527456A>T NCBI36
NG_011485.1:g.43886A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.1599+4A>T MANE Select ENSP00000369442.3:n.1599+4A>T
ENST00000380099.3:c.1599+4A>T ENSP00000369442.3:n.1599+4A>T
ENST00000487852.1:n.1611A>T
NM_004795.3:c.1599+4A>T NP_004786.2:n.1599+4A>T
XM_006719895.1:c.678+4A>T XP_006719958.1:n.678+4A>T
XM_006719895.2:c.678+4A>T XP_006719958.1:n.678+4A>T
NM_004795.4:c.1599+4A>T MANE Select NP_004786.2:n.1599+4A>T