Canonical Allele Identifier: CA232822017

Gene: KLRC1

Linked Data

• dbSNP Id: rs143299847
• gnomAD v2: 12-10598701-AAAATC-A
• gnomAD v3: 12-10446102-AAAATC-A
• gnomAD v4: 12-10446102-AAAATC-A
• MyVariant Identifiers: chr12:g.10598702_10598706del (hg19) ; chr12:g.10446103_10446107del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10446105_10446109del , CM000674.2:g.10446105_10446109del	GRCh38
NC_000012.11:g.10598704_10598708del , CM000674.1:g.10598704_10598708del	GRCh37
NC_000012.10:g.10489971_10489975del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359151.8:c.*444_*448del MANE Select	ENSP00000352064.3:n.*444_*448del
ENST00000347831.9:c.*444_*448del	ENSP00000256965.7:n.*444_*448del
ENST00000359151.7:c.*444_*448del	ENSP00000352064.3:n.*444_*448del
ENST00000408006.7:c.*444_*448del	ENSP00000385304.3:n.*444_*448del
ENST00000536188.5:c.685+461_685+465del	ENSP00000441432.1:n.685+461_685+465del
ENST00000544822.2:c.*444_*448del	ENSP00000438038.1:n.*444_*448del
NM_001304448.1:c.685+461_685+465del	NP_001291377.1:n.685+461_685+465del
NM_002259.4:c.*444_*448del	NP_002250.1:n.*444_*448del
NM_007328.3:c.*444_*448del	NP_015567.1:n.*444_*448del
NM_213657.2:c.*444_*448del	NP_998822.1:n.*444_*448del
NM_213658.2:c.*444_*448del	NP_998823.1:n.*444_*448del
XM_024448973.1:c.685+461_685+465del	XP_024304741.1:n.685+461_685+465del
NM_002259.5:c.*444_*448del MANE Select	NP_002250.2:n.*444_*448del
NM_007328.4:c.*444_*448del	NP_015567.2:n.*444_*448del
NM_213657.3:c.*444_*448del	NP_998822.2:n.*444_*448del
NM_213658.3:c.*444_*448del	NP_998823.2:n.*444_*448del