Canonical Allele Identifier: CA2083143057

Gene: KL

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.33036381C= , CM000675.2:g.33036381C=	GRCh38
NC_000013.10:g.33610518C= , CM000675.1:g.33610518C=	GRCh37
NC_000013.9:g.32508518C=	NCBI36
NG_011485.1:g.24948C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380099.4:c.820-17386C= MANE Select	ENSP00000369442.3:n.820-17386C=
ENST00000380099.3:c.820-17386C=	ENSP00000369442.3:n.820-17386C=
ENST00000487852.1:n.828-17386C=
NM_004795.3:c.820-17386C=	NP_004786.2:n.820-17386C=
XM_006719895.1:c.-102-17386C=	XP_006719958.1:n.-102-17386C=
XM_006719895.2:c.-102-17386C=	XP_006719958.1:n.-102-17386C=
NM_004795.4:c.820-17386C= MANE Select	NP_004786.2:n.820-17386C=