Canonical Allele Identifier: CA2083135989

Gene: KL

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.33055595T= , CM000675.2:g.33055595T=	GRCh38
NC_000013.10:g.33629732T= , CM000675.1:g.33629732T=	GRCh37
NC_000013.9:g.32527732T=	NCBI36
NG_011485.1:g.44162T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380099.4:c.1599+280T= MANE Select	ENSP00000369442.3:n.1599+280T=
ENST00000380099.3:c.1599+280T=	ENSP00000369442.3:n.1599+280T=
ENST00000487852.1:n.1657+230T=
NM_004795.3:c.1599+280T=	NP_004786.2:n.1599+280T=
XM_006719895.1:c.678+280T=	XP_006719958.1:n.678+280T=
XM_006719895.2:c.678+280T=	XP_006719958.1:n.678+280T=
NM_004795.4:c.1599+280T= MANE Select	NP_004786.2:n.1599+280T=