Canonical Allele Identifier: CA2083135390

Gene: KL

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.33055144C= , CM000675.2:g.33055144C=	GRCh38
NC_000013.10:g.33629281C= , CM000675.1:g.33629281C=	GRCh37
NC_000013.9:g.32527281C=	NCBI36
NG_011485.1:g.43711C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380099.4:c.1428C= MANE Select	ENSP00000369442.3:p.Leu476=
ENST00000380099.3:c.1428C=	ENSP00000369442.3:p.Leu476=
ENST00000487852.1:n.1436C=
NM_004795.3:c.1428C=	NP_004786.2:p.Leu476=
XM_006719895.1:c.507C=	XP_006719958.1:p.Leu169=
XM_006719895.2:c.507C=	XP_006719958.1:p.Leu169=
NM_004795.4:c.1428C= MANE Select	NP_004786.2:p.Leu476=