Canonical Allele Identifier: CA2083133493

Gene: KL

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.33053928T= , CM000675.2:g.33053928T=	GRCh38
NC_000013.10:g.33628065T= , CM000675.1:g.33628065T=	GRCh37
NC_000013.9:g.32526065T=	NCBI36
NG_011485.1:g.42495T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380099.4:c.981T= MANE Select	ENSP00000369442.3:p.Phe327=
ENST00000380099.3:c.981T=	ENSP00000369442.3:p.Phe327=
ENST00000487852.1:n.989T=
NM_004795.3:c.981T=	NP_004786.2:p.Phe327=
XM_006719895.1:c.60T=	XP_006719958.1:p.Phe20=
XM_006719895.2:c.60T=	XP_006719958.1:p.Phe20=
NM_004795.4:c.981T= MANE Select	NP_004786.2:p.Phe327=