Canonical Allele Identifier: CA2083135468

Gene: KL

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.33055212A= , CM000675.2:g.33055212A=	GRCh38
NC_000013.10:g.33629349A= , CM000675.1:g.33629349A=	GRCh37
NC_000013.9:g.32527349A=	NCBI36
NG_011485.1:g.43779A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380099.4:c.1496A= MANE Select	ENSP00000369442.3:p.Lys499=
ENST00000380099.3:c.1496A=	ENSP00000369442.3:p.Lys499=
ENST00000487852.1:n.1504A=
NM_004795.3:c.1496A=	NP_004786.2:p.Lys499=
XM_006719895.1:c.575A=	XP_006719958.1:p.Lys192=
XM_006719895.2:c.575A=	XP_006719958.1:p.Lys192=
NM_004795.4:c.1496A= MANE Select	NP_004786.2:p.Lys499=