Canonical Allele Identifier: CA442643863
Gene: KLKB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187178441G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186257287G>A , CM000666.2:g.186257287G>A GRCh38
NC_000004.11:g.187178441G>A , CM000666.1:g.187178441G>A GRCh37
NC_000004.10:g.187415435G>A NCBI36
NG_012095.2:g.53309G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264690.11:c.1647G>A MANE Select ENSP00000264690.6:p.Gln549=
ENST00000264690.10:c.1647G>A ENSP00000264690.6:p.Gln549=
ENST00000511406.5:n.1708G>A
ENST00000511608.5:c.1790G>A
ENST00000513864.2:c.1472-734G>A ENSP00000424469.2:n.1472-734G>A
NM_000892.3:c.1647G>A NP_000883.2:p.Gln549=
XM_011531930.1:c.1680G>A XP_011530232.1:p.Gln560=
XM_011531931.1:c.1680G>A XP_011530233.1:p.Gln560=
XM_011531932.1:c.1566G>A XP_011530234.1:p.Gln522=
XM_011531933.1:c.1566G>A XP_011530235.1:p.Gln522=
XM_011531934.1:c.1041G>A XP_011530236.1:p.Gln347=
NM_000892.4:c.1647G>A NP_000883.2:p.Gln549=
NM_001318394.1:c.1472-734G>A NP_001305323.1:n.1472-734G>A
NM_001318396.1:c.1041G>A NP_001305325.1:p.Gln347=
XM_011531930.2:c.1680G>A XP_011530232.1:p.Gln560=
XM_017008181.1:c.1680G>A XP_016863670.1:p.Gln560=
XM_017008182.1:c.1619-734G>A XP_016863671.1:n.1619-734G>A
XM_017008183.1:c.1586-734G>A XP_016863672.1:n.1586-734G>A
XM_017008184.1:c.1041G>A XP_016863673.1:p.Gln347=
NM_000892.5:c.1647G>A MANE Select NP_000883.2:p.Gln549=
NM_001318394.2:c.1472-734G>A NP_001305323.1:n.1472-734G>A
NM_001318396.2:c.1041G>A NP_001305325.1:p.Gln347=