Canonical Allele Identifier: CA2083135736
Gene: KL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33055372A= , CM000675.2:g.33055372A= GRCh38
NC_000013.10:g.33629509A= , CM000675.1:g.33629509A= GRCh37
NC_000013.9:g.32527509A= NCBI36
NG_011485.1:g.43939A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.1599+57A= MANE Select ENSP00000369442.3:n.1599+57A=
ENST00000380099.3:c.1599+57A= ENSP00000369442.3:n.1599+57A=
ENST00000487852.1:n.1657+7A=
NM_004795.3:c.1599+57A= NP_004786.2:n.1599+57A=
XM_006719895.1:c.678+57A= XP_006719958.1:n.678+57A=
XM_006719895.2:c.678+57A= XP_006719958.1:n.678+57A=
NM_004795.4:c.1599+57A= MANE Select NP_004786.2:n.1599+57A=
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