Canonical Allele Identifier: CA2015950203

Gene: KLRC1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10446109A= , CM000674.2:g.10446109A=	GRCh38
NC_000012.11:g.10598708A= , CM000674.1:g.10598708A=	GRCh37
NC_000012.10:g.10489975A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359151.8:c.*442T= MANE Select	ENSP00000352064.3:n.*442T=
ENST00000347831.9:c.*442T=	ENSP00000256965.7:n.*442T=
ENST00000359151.7:c.*442T=	ENSP00000352064.3:n.*442T=
ENST00000408006.7:c.*442T=	ENSP00000385304.3:n.*442T=
ENST00000536188.5:c.685+459T=	ENSP00000441432.1:n.685+459T=
ENST00000544822.2:c.*442T=	ENSP00000438038.1:n.*442T=
NM_001304448.1:c.685+459T=	NP_001291377.1:n.685+459T=
NM_002259.4:c.*442T=	NP_002250.1:n.*442T=
NM_007328.3:c.*442T=	NP_015567.1:n.*442T=
NM_213657.2:c.*442T=	NP_998822.1:n.*442T=
NM_213658.2:c.*442T=	NP_998823.1:n.*442T=
XM_024448973.1:c.685+459T=	XP_024304741.1:n.685+459T=
NM_002259.5:c.*442T= MANE Select	NP_002250.2:n.*442T=
NM_007328.4:c.*442T=	NP_015567.2:n.*442T=
NM_213657.3:c.*442T=	NP_998822.2:n.*442T=
NM_213658.3:c.*442T=	NP_998823.2:n.*442T=