Canonical Allele Identifier: CA2083135971
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33055570C= , CM000675.2:g.33055570C= GRCh38
NC_000013.10:g.33629707C= , CM000675.1:g.33629707C= GRCh37
NC_000013.9:g.32527707C= NCBI36
NG_011485.1:g.44137C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.1599+255C= MANE Select ENSP00000369442.3:n.1599+255C=
ENST00000380099.3:c.1599+255C= ENSP00000369442.3:n.1599+255C=
ENST00000487852.1:n.1657+205C=
NM_004795.3:c.1599+255C= NP_004786.2:n.1599+255C=
XM_006719895.1:c.678+255C= XP_006719958.1:n.678+255C=
XM_006719895.2:c.678+255C= XP_006719958.1:n.678+255C=
NM_004795.4:c.1599+255C= MANE Select NP_004786.2:n.1599+255C=