Canonical Allele Identifier: CA2083135786
Gene: KL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33055406T= , CM000675.2:g.33055406T= GRCh38
NC_000013.10:g.33629543T= , CM000675.1:g.33629543T= GRCh37
NC_000013.9:g.32527543T= NCBI36
NG_011485.1:g.43973T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.1599+91T= MANE Select ENSP00000369442.3:n.1599+91T=
ENST00000380099.3:c.1599+91T= ENSP00000369442.3:n.1599+91T=
ENST00000487852.1:n.1657+41T=
NM_004795.3:c.1599+91T= NP_004786.2:n.1599+91T=
XM_006719895.1:c.678+91T= XP_006719958.1:n.678+91T=
XM_006719895.2:c.678+91T= XP_006719958.1:n.678+91T=
NM_004795.4:c.1599+91T= MANE Select NP_004786.2:n.1599+91T=
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