Canonical Allele Identifier: CA2083133466

Gene: KL

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.33053921G= , CM000675.2:g.33053921G=	GRCh38
NC_000013.10:g.33628058G= , CM000675.1:g.33628058G=	GRCh37
NC_000013.9:g.32526058G=	NCBI36
NG_011485.1:g.42488G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380099.4:c.974G= MANE Select	ENSP00000369442.3:p.Gly325=
ENST00000380099.3:c.974G=	ENSP00000369442.3:p.Gly325=
ENST00000487852.1:n.982G=
NM_004795.3:c.974G=	NP_004786.2:p.Gly325=
XM_006719895.1:c.53G=	XP_006719958.1:p.Gly18=
XM_006719895.2:c.53G=	XP_006719958.1:p.Gly18=
NM_004795.4:c.974G= MANE Select	NP_004786.2:p.Gly325=