Canonical Allele Identifier: CA2083136006
Gene: KL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33055631G= , CM000675.2:g.33055631G= GRCh38
NC_000013.10:g.33629768G= , CM000675.1:g.33629768G= GRCh37
NC_000013.9:g.32527768G= NCBI36
NG_011485.1:g.44198G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.1599+316G= MANE Select ENSP00000369442.3:n.1599+316G=
ENST00000380099.3:c.1599+316G= ENSP00000369442.3:n.1599+316G=
ENST00000487852.1:n.1657+266G=
NM_004795.3:c.1599+316G= NP_004786.2:n.1599+316G=
XM_006719895.1:c.678+316G= XP_006719958.1:n.678+316G=
XM_006719895.2:c.678+316G= XP_006719958.1:n.678+316G=
NM_004795.4:c.1599+316G= MANE Select NP_004786.2:n.1599+316G=
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