Canonical Allele Identifier: CA682974735

Gene: KLRC1

Linked Data

• dbSNP Id: rs60767265
• gnomAD v3: 12-10446027-CTTT-C
• gnomAD v4: 12-10446027-CTTT-C
• MyVariant Identifiers: chr12:g.10598627_10598629del (hg19) ; chr12:g.10446028_10446030del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10446038_10446040del , CM000674.2:g.10446038_10446040del	GRCh38
NC_000012.11:g.10598637_10598639del , CM000674.1:g.10598637_10598639del	GRCh37
NC_000012.10:g.10489904_10489906del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359151.8:c.*521_*523del MANE Select	ENSP00000352064.3:n.*521_*523del
ENST00000359151.7:c.*521_*523del	ENSP00000352064.3:n.*521_*523del
ENST00000408006.7:c.*521_*523del	ENSP00000385304.3:n.*521_*523del
ENST00000536188.5:c.685+538_685+540del	ENSP00000441432.1:n.685+538_685+540del
NM_001304448.1:c.685+538_685+540del	NP_001291377.1:n.685+538_685+540del
NM_002259.4:c.*521_*523del	NP_002250.1:n.*521_*523del
NM_007328.3:c.*521_*523del	NP_015567.1:n.*521_*523del
NM_213657.2:c.*521_*523del	NP_998822.1:n.*521_*523del
NM_213658.2:c.*521_*523del	NP_998823.1:n.*521_*523del
XM_024448973.1:c.685+538_685+540del	XP_024304741.1:n.685+538_685+540del
NM_002259.5:c.*521_*523del MANE Select	NP_002250.2:n.*521_*523del
NM_007328.4:c.*521_*523del	NP_015567.2:n.*521_*523del
NM_213657.3:c.*521_*523del	NP_998822.2:n.*521_*523del
NM_213658.3:c.*521_*523del	NP_998823.2:n.*521_*523del