Canonical Allele Identifier: CA2083135416

Gene: KL

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.33055168G= , CM000675.2:g.33055168G=	GRCh38
NC_000013.10:g.33629305G= , CM000675.1:g.33629305G=	GRCh37
NC_000013.9:g.32527305G=	NCBI36
NG_011485.1:g.43735G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380099.4:c.1452G= MANE Select	ENSP00000369442.3:p.Gln484=
ENST00000380099.3:c.1452G=	ENSP00000369442.3:p.Gln484=
ENST00000487852.1:n.1460G=
NM_004795.3:c.1452G=	NP_004786.2:p.Gln484=
XM_006719895.1:c.531G=	XP_006719958.1:p.Gln177=
XM_006719895.2:c.531G=	XP_006719958.1:p.Gln177=
NM_004795.4:c.1452G= MANE Select	NP_004786.2:p.Gln484=