Canonical Allele Identifier: CA1519902163
Gene: KLKB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186236717G= , CM000666.2:g.186236717G= GRCh38
NC_000004.11:g.187157871G= , CM000666.1:g.187157871G= GRCh37
NC_000004.10:g.187394865G= NCBI36
NG_012095.2:g.32739G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264690.11:c.329-64G= MANE Select ENSP00000264690.6:n.329-64G=
ENST00000264690.10:c.329-64G= ENSP00000264690.6:n.329-64G=
ENST00000428196.5:c.329-64G= ENSP00000412366.1:n.329-64G=
ENST00000446598.6:c.215-64G= ENSP00000415563.2:n.215-64G=
ENST00000511406.5:n.359-64G=
ENST00000511608.5:c.472-64G=
ENST00000513864.2:c.215-64G= ENSP00000424469.2:n.215-64G=
NM_000892.3:c.329-64G= NP_000883.2:n.329-64G=
XM_011531930.1:c.329-64G= XP_011530232.1:n.329-64G=
XM_011531931.1:c.329-64G= XP_011530233.1:n.329-64G=
XM_011531932.1:c.215-64G= XP_011530234.1:n.215-64G=
XM_011531933.1:c.215-64G= XP_011530235.1:n.215-64G=
XM_011531934.1:c.-309-64G= XP_011530236.1:n.-309-64G=
NM_000892.4:c.329-64G= NP_000883.2:n.329-64G=
NM_001318394.1:c.215-64G= NP_001305323.1:n.215-64G=
NM_001318396.1:c.-309-64G= NP_001305325.1:n.-309-64G=
XM_011531930.2:c.329-64G= XP_011530232.1:n.329-64G=
XM_017008181.1:c.329-64G= XP_016863670.1:n.329-64G=
XM_017008182.1:c.329-64G= XP_016863671.1:n.329-64G=
XM_017008183.1:c.329-64G= XP_016863672.1:n.329-64G=
NM_000892.5:c.329-64G= MANE Select NP_000883.2:n.329-64G=
NM_001318394.2:c.215-64G= NP_001305323.1:n.215-64G=
NM_001318396.2:c.-309-64G= NP_001305325.1:n.-309-64G=