Canonical Allele Identifier: CA2083135485

Gene: KL

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.33055221A= , CM000675.2:g.33055221A=	GRCh38
NC_000013.10:g.33629358A= , CM000675.1:g.33629358A=	GRCh37
NC_000013.9:g.32527358A=	NCBI36
NG_011485.1:g.43788A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380099.4:c.1505A= MANE Select	ENSP00000369442.3:p.Glu502=
ENST00000380099.3:c.1505A=	ENSP00000369442.3:p.Glu502=
ENST00000487852.1:n.1513A=
NM_004795.3:c.1505A=	NP_004786.2:p.Glu502=
XM_006719895.1:c.584A=	XP_006719958.1:p.Glu195=
XM_006719895.2:c.584A=	XP_006719958.1:p.Glu195=
NM_004795.4:c.1505A= MANE Select	NP_004786.2:p.Glu502=