Canonical Allele Identifier: CA2083133652

Gene: KL

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.33053976T= , CM000675.2:g.33053976T=	GRCh38
NC_000013.10:g.33628113T= , CM000675.1:g.33628113T=	GRCh37
NC_000013.9:g.32526113T=	NCBI36
NG_011485.1:g.42543T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380099.4:c.1029T= MANE Select	ENSP00000369442.3:p.Asn343=
ENST00000380099.3:c.1029T=	ENSP00000369442.3:p.Asn343=
ENST00000487852.1:n.1037T=
NM_004795.3:c.1029T=	NP_004786.2:p.Asn343=
XM_006719895.1:c.108T=	XP_006719958.1:p.Asn36=
XM_006719895.2:c.108T=	XP_006719958.1:p.Asn36=
NM_004795.4:c.1029T= MANE Select	NP_004786.2:p.Asn343=