Canonical Allele Identifier: CA603270097

Gene: KLRC1

Linked Data

• dbSNP Id: rs1414874756
• gnomAD v2: 12-10598663-G-A
• gnomAD v3: 12-10446064-G-A
• gnomAD v4: 12-10446064-G-A
• MyVariant Identifiers: chr12:g.10598663G>A (hg19) ; chr12:g.10446064G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10446064G>A , CM000674.2:g.10446064G>A	GRCh38
NC_000012.11:g.10598663G>A , CM000674.1:g.10598663G>A	GRCh37
NC_000012.10:g.10489930G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359151.8:c.*487C>T MANE Select	ENSP00000352064.3:n.*487C>T
ENST00000347831.9:c.*487C>T	ENSP00000256965.7:n.*487C>T
ENST00000359151.7:c.*487C>T	ENSP00000352064.3:n.*487C>T
ENST00000408006.7:c.*487C>T	ENSP00000385304.3:n.*487C>T
ENST00000536188.5:c.685+504C>T	ENSP00000441432.1:n.685+504C>T
ENST00000544822.2:c.*487C>T	ENSP00000438038.1:n.*487C>T
NM_001304448.1:c.685+504C>T	NP_001291377.1:n.685+504C>T
NM_002259.4:c.*487C>T	NP_002250.1:n.*487C>T
NM_007328.3:c.*487C>T	NP_015567.1:n.*487C>T
NM_213657.2:c.*487C>T	NP_998822.1:n.*487C>T
NM_213658.2:c.*487C>T	NP_998823.1:n.*487C>T
XM_024448973.1:c.685+504C>T	XP_024304741.1:n.685+504C>T
NM_002259.5:c.*487C>T MANE Select	NP_002250.2:n.*487C>T
NM_007328.4:c.*487C>T	NP_015567.2:n.*487C>T
NM_213657.3:c.*487C>T	NP_998822.2:n.*487C>T
NM_213658.3:c.*487C>T	NP_998823.2:n.*487C>T