Canonical Allele Identifier: CA358945186
Gene: KLKB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186236865A>G , CM000666.2:g.186236865A>G GRCh38
NC_000004.11:g.187158019A>G , CM000666.1:g.187158019A>G GRCh37
NC_000004.10:g.187395013A>G NCBI36
NG_012095.2:g.32887A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264690.11:c.413A>G MANE Select ENSP00000264690.6:p.Gln138Arg
ENST00000264690.10:c.413A>G ENSP00000264690.6:p.Gln138Arg
ENST00000428196.5:c.413A>G ENSP00000412366.1:p.Gln138Arg
ENST00000446598.6:c.299A>G ENSP00000415563.2:p.Gln100Arg
ENST00000511406.5:n.443A>G
ENST00000511608.5:c.556A>G
ENST00000513864.2:c.299A>G ENSP00000424469.2:p.Gln100Arg
NM_000892.3:c.413A>G NP_000883.2:p.Gln138Arg
XM_011531930.1:c.413A>G XP_011530232.1:p.Gln138Arg
XM_011531931.1:c.413A>G XP_011530233.1:p.Gln138Arg
XM_011531932.1:c.299A>G XP_011530234.1:p.Gln100Arg
XM_011531933.1:c.299A>G XP_011530235.1:p.Gln100Arg
XM_011531934.1:c.-225A>G XP_011530236.1:n.-225A>G
NM_000892.4:c.413A>G NP_000883.2:p.Gln138Arg
NM_001318394.1:c.299A>G NP_001305323.1:p.Gln100Arg
NM_001318396.1:c.-225A>G NP_001305325.1:n.-225A>G
XM_011531930.2:c.413A>G XP_011530232.1:p.Gln138Arg
XM_017008181.1:c.413A>G XP_016863670.1:p.Gln138Arg
XM_017008182.1:c.413A>G XP_016863671.1:p.Gln138Arg
XM_017008183.1:c.413A>G XP_016863672.1:p.Gln138Arg
NM_000892.5:c.413A>G MANE Select NP_000883.2:p.Gln138Arg
NM_001318394.2:c.299A>G NP_001305323.1:p.Gln100Arg
NM_001318396.2:c.-225A>G NP_001305325.1:n.-225A>G