Canonical Allele Identifier: CA603269951

Gene: KLRC1

Linked Data

• dbSNP Id: rs1406937151
• gnomAD v2: 12-10598662-C-T
• gnomAD v3: 12-10446063-C-T
• gnomAD v4: 12-10446063-C-T
• MyVariant Identifiers: chr12:g.10598662C>T (hg19) ; chr12:g.10446063C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10446063C>T , CM000674.2:g.10446063C>T	GRCh38
NC_000012.11:g.10598662C>T , CM000674.1:g.10598662C>T	GRCh37
NC_000012.10:g.10489929C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359151.8:c.*488G>A MANE Select	ENSP00000352064.3:n.*488G>A
ENST00000347831.9:c.*488G>A	ENSP00000256965.7:n.*488G>A
ENST00000359151.7:c.*488G>A	ENSP00000352064.3:n.*488G>A
ENST00000408006.7:c.*488G>A	ENSP00000385304.3:n.*488G>A
ENST00000536188.5:c.685+505G>A	ENSP00000441432.1:n.685+505G>A
ENST00000544822.2:c.*488G>A	ENSP00000438038.1:n.*488G>A
NM_001304448.1:c.685+505G>A	NP_001291377.1:n.685+505G>A
NM_002259.4:c.*488G>A	NP_002250.1:n.*488G>A
NM_007328.3:c.*488G>A	NP_015567.1:n.*488G>A
NM_213657.2:c.*488G>A	NP_998822.1:n.*488G>A
NM_213658.2:c.*488G>A	NP_998823.1:n.*488G>A
XM_024448973.1:c.685+505G>A	XP_024304741.1:n.685+505G>A
NM_002259.5:c.*488G>A MANE Select	NP_002250.2:n.*488G>A
NM_007328.4:c.*488G>A	NP_015567.2:n.*488G>A
NM_213657.3:c.*488G>A	NP_998822.2:n.*488G>A
NM_213658.3:c.*488G>A	NP_998823.2:n.*488G>A