Canonical Allele Identifier: CA3163027
Gene: KLKB1 HGNC NCBI

Linked Data

dbSNP Id: rs202142549

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186236790G>A , CM000666.2:g.186236790G>A GRCh38
NC_000004.11:g.187157944G>A , CM000666.1:g.187157944G>A GRCh37
NC_000004.10:g.187394938G>A NCBI36
NG_012095.2:g.32812G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264690.11:c.338G>A MANE Select ENSP00000264690.6:p.Arg113Gln
ENST00000264690.10:c.338G>A ENSP00000264690.6:p.Arg113Gln
ENST00000428196.5:c.338G>A ENSP00000412366.1:p.Arg113Gln
ENST00000446598.6:c.224G>A ENSP00000415563.2:p.Arg75Gln
ENST00000511406.5:n.368G>A
ENST00000511608.5:c.481G>A
ENST00000513864.2:c.224G>A ENSP00000424469.2:p.Arg75Gln
NM_000892.3:c.338G>A NP_000883.2:p.Arg113Gln
XM_011531930.1:c.338G>A XP_011530232.1:p.Arg113Gln
XM_011531931.1:c.338G>A XP_011530233.1:p.Arg113Gln
XM_011531932.1:c.224G>A XP_011530234.1:p.Arg75Gln
XM_011531933.1:c.224G>A XP_011530235.1:p.Arg75Gln
XM_011531934.1:c.-300G>A XP_011530236.1:n.-300G>A
NM_000892.4:c.338G>A NP_000883.2:p.Arg113Gln
NM_001318394.1:c.224G>A NP_001305323.1:p.Arg75Gln
NM_001318396.1:c.-300G>A NP_001305325.1:n.-300G>A
XM_011531930.2:c.338G>A XP_011530232.1:p.Arg113Gln
XM_017008181.1:c.338G>A XP_016863670.1:p.Arg113Gln
XM_017008182.1:c.338G>A XP_016863671.1:p.Arg113Gln
XM_017008183.1:c.338G>A XP_016863672.1:p.Arg113Gln
NM_000892.5:c.338G>A MANE Select NP_000883.2:p.Arg113Gln
NM_001318394.2:c.224G>A NP_001305323.1:p.Arg75Gln
NM_001318396.2:c.-300G>A NP_001305325.1:n.-300G>A