Canonical Allele Identifier: CA2672900100
Gene: KLKB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186257118_186257125del , CM000666.2:g.186257118_186257125del GRCh38
NC_000004.11:g.187178272_187178279del , CM000666.1:g.187178272_187178279del GRCh37
NC_000004.10:g.187415266_187415273del NCBI36
NG_012095.2:g.53140_53147del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264690.11:c.1586-108_1586-101del MANE Select ENSP00000264690.6:n.1586-108_1586-101del
ENST00000264690.10:c.1586-108_1586-101del ENSP00000264690.6:n.1586-108_1586-101del
ENST00000511406.5:n.1647-108_1647-101del
ENST00000511608.5:c.1729-108_1729-101del
ENST00000513864.2:c.1472-903_1472-896del ENSP00000424469.2:n.1472-903_1472-896del
NM_000892.3:c.1586-108_1586-101del NP_000883.2:n.1586-108_1586-101del
XM_011531930.1:c.1619-108_1619-101del XP_011530232.1:n.1619-108_1619-101del
XM_011531931.1:c.1619-108_1619-101del XP_011530233.1:n.1619-108_1619-101del
XM_011531932.1:c.1505-108_1505-101del XP_011530234.1:n.1505-108_1505-101del
XM_011531933.1:c.1505-108_1505-101del XP_011530235.1:n.1505-108_1505-101del
XM_011531934.1:c.980-108_980-101del XP_011530236.1:n.980-108_980-101del
NM_000892.4:c.1586-108_1586-101del NP_000883.2:n.1586-108_1586-101del
NM_001318394.1:c.1472-903_1472-896del NP_001305323.1:n.1472-903_1472-896del
NM_001318396.1:c.980-108_980-101del NP_001305325.1:n.980-108_980-101del
XM_011531930.2:c.1619-108_1619-101del XP_011530232.1:n.1619-108_1619-101del
XM_017008181.1:c.1619-108_1619-101del XP_016863670.1:n.1619-108_1619-101del
XM_017008182.1:c.1619-903_1619-896del XP_016863671.1:n.1619-903_1619-896del
XM_017008183.1:c.1586-903_1586-896del XP_016863672.1:n.1586-903_1586-896del
XM_017008184.1:c.980-108_980-101del XP_016863673.1:n.980-108_980-101del
NM_000892.5:c.1586-108_1586-101del MANE Select NP_000883.2:n.1586-108_1586-101del
NM_001318394.2:c.1472-903_1472-896del NP_001305323.1:n.1472-903_1472-896del
NM_001318396.2:c.980-108_980-101del NP_001305325.1:n.980-108_980-101del