Canonical Allele Identifier: CA2672900108
Gene: KLKB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186257134_186257176del , CM000666.2:g.186257134_186257176del GRCh38
NC_000004.11:g.187178288_187178330del , CM000666.1:g.187178288_187178330del GRCh37
NC_000004.10:g.187415282_187415324del NCBI36
NG_012095.2:g.53156_53198del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264690.11:c.1586-92_1586-50del MANE Select ENSP00000264690.6:n.1586-92_1586-50del
ENST00000264690.10:c.1586-92_1586-50del ENSP00000264690.6:n.1586-92_1586-50del
ENST00000511406.5:n.1647-92_1647-50del
ENST00000511608.5:c.1729-92_1729-50del
ENST00000513864.2:c.1472-887_1472-845del ENSP00000424469.2:n.1472-887_1472-845del
NM_000892.3:c.1586-92_1586-50del NP_000883.2:n.1586-92_1586-50del
XM_011531930.1:c.1619-92_1619-50del XP_011530232.1:n.1619-92_1619-50del
XM_011531931.1:c.1619-92_1619-50del XP_011530233.1:n.1619-92_1619-50del
XM_011531932.1:c.1505-92_1505-50del XP_011530234.1:n.1505-92_1505-50del
XM_011531933.1:c.1505-92_1505-50del XP_011530235.1:n.1505-92_1505-50del
XM_011531934.1:c.980-92_980-50del XP_011530236.1:n.980-92_980-50del
NM_000892.4:c.1586-92_1586-50del NP_000883.2:n.1586-92_1586-50del
NM_001318394.1:c.1472-887_1472-845del NP_001305323.1:n.1472-887_1472-845del
NM_001318396.1:c.980-92_980-50del NP_001305325.1:n.980-92_980-50del
XM_011531930.2:c.1619-92_1619-50del XP_011530232.1:n.1619-92_1619-50del
XM_017008181.1:c.1619-92_1619-50del XP_016863670.1:n.1619-92_1619-50del
XM_017008182.1:c.1619-887_1619-845del XP_016863671.1:n.1619-887_1619-845del
XM_017008183.1:c.1586-887_1586-845del XP_016863672.1:n.1586-887_1586-845del
XM_017008184.1:c.980-92_980-50del XP_016863673.1:n.980-92_980-50del
NM_000892.5:c.1586-92_1586-50del MANE Select NP_000883.2:n.1586-92_1586-50del
NM_001318394.2:c.1472-887_1472-845del NP_001305323.1:n.1472-887_1472-845del
NM_001318396.2:c.980-92_980-50del NP_001305325.1:n.980-92_980-50del