Canonical Allele Identifier: CA2083136018
Gene: KL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33055642T= , CM000675.2:g.33055642T= GRCh38
NC_000013.10:g.33629779T= , CM000675.1:g.33629779T= GRCh37
NC_000013.9:g.32527779T= NCBI36
NG_011485.1:g.44209T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.1599+327T= MANE Select ENSP00000369442.3:n.1599+327T=
ENST00000380099.3:c.1599+327T= ENSP00000369442.3:n.1599+327T=
ENST00000487852.1:n.1657+277T=
NM_004795.3:c.1599+327T= NP_004786.2:n.1599+327T=
XM_006719895.1:c.678+327T= XP_006719958.1:n.678+327T=
XM_006719895.2:c.678+327T= XP_006719958.1:n.678+327T=
NM_004795.4:c.1599+327T= MANE Select NP_004786.2:n.1599+327T=
Search 100 bp 5'
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