Canonical Allele Identifier: CA442640154
Gene: KLKB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187157936T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186236782T>A , CM000666.2:g.186236782T>A GRCh38
NC_000004.11:g.187157936T>A , CM000666.1:g.187157936T>A GRCh37
NC_000004.10:g.187394930T>A NCBI36
NG_012095.2:g.32804T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264690.11:c.330T>A MANE Select ENSP00000264690.6:p.Ala110=
ENST00000264690.10:c.330T>A ENSP00000264690.6:p.Ala110=
ENST00000428196.5:c.330T>A ENSP00000412366.1:p.Ala110=
ENST00000446598.6:c.216T>A ENSP00000415563.2:p.Ala72=
ENST00000511406.5:n.360T>A
ENST00000511608.5:c.473T>A
ENST00000513864.2:c.216T>A ENSP00000424469.2:p.Ala72=
NM_000892.3:c.330T>A NP_000883.2:p.Ala110=
XM_011531930.1:c.330T>A XP_011530232.1:p.Ala110=
XM_011531931.1:c.330T>A XP_011530233.1:p.Ala110=
XM_011531932.1:c.216T>A XP_011530234.1:p.Ala72=
XM_011531933.1:c.216T>A XP_011530235.1:p.Ala72=
XM_011531934.1:c.-308T>A XP_011530236.1:n.-308T>A
NM_000892.4:c.330T>A NP_000883.2:p.Ala110=
NM_001318394.1:c.216T>A NP_001305323.1:p.Ala72=
NM_001318396.1:c.-308T>A NP_001305325.1:n.-308T>A
XM_011531930.2:c.330T>A XP_011530232.1:p.Ala110=
XM_017008181.1:c.330T>A XP_016863670.1:p.Ala110=
XM_017008182.1:c.330T>A XP_016863671.1:p.Ala110=
XM_017008183.1:c.330T>A XP_016863672.1:p.Ala110=
NM_000892.5:c.330T>A MANE Select NP_000883.2:p.Ala110=
NM_001318394.2:c.216T>A NP_001305323.1:p.Ala72=
NM_001318396.2:c.-308T>A NP_001305325.1:n.-308T>A