Canonical Allele Identifier: CA2832294675
Gene: KLRC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.10446066_10446067insGG , CM000674.2:g.10446066_10446067insGG GRCh38
NC_000012.11:g.10598665_10598666insGG , CM000674.1:g.10598665_10598666insGG GRCh37
NC_000012.10:g.10489932_10489933insGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359151.8:c.*485_*486insCC MANE Select ENSP00000352064.3:n.*485_*486insCC
ENST00000347831.9:c.*485_*486insCC ENSP00000256965.7:n.*485_*486insCC
ENST00000359151.7:c.*485_*486insCC ENSP00000352064.3:n.*485_*486insCC
ENST00000408006.7:c.*485_*486insCC ENSP00000385304.3:n.*485_*486insCC
ENST00000536188.5:c.685+502_685+503insCC ENSP00000441432.1:n.685+502_685+503insCC
ENST00000544822.2:c.*485_*486insCC ENSP00000438038.1:n.*485_*486insCC
NM_001304448.1:c.685+502_685+503insCC NP_001291377.1:n.685+502_685+503insCC
NM_002259.4:c.*485_*486insCC NP_002250.1:n.*485_*486insCC
NM_007328.3:c.*485_*486insCC NP_015567.1:n.*485_*486insCC
NM_213657.2:c.*485_*486insCC NP_998822.1:n.*485_*486insCC
NM_213658.2:c.*485_*486insCC NP_998823.1:n.*485_*486insCC
XM_024448973.1:c.685+502_685+503insCC XP_024304741.1:n.685+502_685+503insCC
NM_002259.5:c.*485_*486insCC MANE Select NP_002250.2:n.*485_*486insCC
NM_007328.4:c.*485_*486insCC NP_015567.2:n.*485_*486insCC
NM_213657.3:c.*485_*486insCC NP_998822.2:n.*485_*486insCC
NM_213658.3:c.*485_*486insCC NP_998823.2:n.*485_*486insCC