Canonical Allele Identifier: CA2794532297

Gene: KLRC1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10446215dup , CM000674.2:g.10446215dup	GRCh38
NC_000012.11:g.10598814dup , CM000674.1:g.10598814dup	GRCh37
NC_000012.10:g.10490081dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359151.8:c.*336dup MANE Select	ENSP00000352064.3:n.*336dup
ENST00000347831.9:c.*336dup	ENSP00000256965.7:n.*336dup
ENST00000359151.7:c.*336dup	ENSP00000352064.3:n.*336dup
ENST00000408006.7:c.*336dup	ENSP00000385304.3:n.*336dup
ENST00000536188.5:c.685+353dup	ENSP00000441432.1:n.685+353dup
ENST00000544822.2:c.*336dup	ENSP00000438038.1:n.*336dup
NM_001304448.1:c.685+353dup	NP_001291377.1:n.685+353dup
NM_002259.4:c.*336dup	NP_002250.1:n.*336dup
NM_007328.3:c.*336dup	NP_015567.1:n.*336dup
NM_213657.2:c.*336dup	NP_998822.1:n.*336dup
NM_213658.2:c.*336dup	NP_998823.1:n.*336dup
XM_024448973.1:c.685+353dup	XP_024304741.1:n.685+353dup
NM_002259.5:c.*336dup MANE Select	NP_002250.2:n.*336dup
NM_007328.4:c.*336dup	NP_015567.2:n.*336dup
NM_213657.3:c.*336dup	NP_998822.2:n.*336dup
NM_213658.3:c.*336dup	NP_998823.2:n.*336dup