Canonical Allele Identifier: CA442640278

Gene: KLKB1

Linked Data

• MyVariant Identifiers: chr4:g.187158008T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186236854T>G , CM000666.2:g.186236854T>G	GRCh38
NC_000004.11:g.187158008T>G , CM000666.1:g.187158008T>G	GRCh37
NC_000004.10:g.187395002T>G	NCBI36
NG_012095.2:g.32876T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264690.11:c.402T>G MANE Select	ENSP00000264690.6:p.Val134=
ENST00000264690.10:c.402T>G	ENSP00000264690.6:p.Val134=
ENST00000428196.5:c.402T>G	ENSP00000412366.1:p.Val134=
ENST00000446598.6:c.288T>G	ENSP00000415563.2:p.Val96=
ENST00000511406.5:n.432T>G
ENST00000511608.5:c.545T>G
ENST00000513864.2:c.288T>G	ENSP00000424469.2:p.Val96=
NM_000892.3:c.402T>G	NP_000883.2:p.Val134=
XM_011531930.1:c.402T>G	XP_011530232.1:p.Val134=
XM_011531931.1:c.402T>G	XP_011530233.1:p.Val134=
XM_011531932.1:c.288T>G	XP_011530234.1:p.Val96=
XM_011531933.1:c.288T>G	XP_011530235.1:p.Val96=
XM_011531934.1:c.-236T>G	XP_011530236.1:n.-236T>G
NM_000892.4:c.402T>G	NP_000883.2:p.Val134=
NM_001318394.1:c.288T>G	NP_001305323.1:p.Val96=
NM_001318396.1:c.-236T>G	NP_001305325.1:n.-236T>G
XM_011531930.2:c.402T>G	XP_011530232.1:p.Val134=
XM_017008181.1:c.402T>G	XP_016863670.1:p.Val134=
XM_017008182.1:c.402T>G	XP_016863671.1:p.Val134=
XM_017008183.1:c.402T>G	XP_016863672.1:p.Val134=
NM_000892.5:c.402T>G MANE Select	NP_000883.2:p.Val134=
NM_001318394.2:c.288T>G	NP_001305323.1:p.Val96=
NM_001318396.2:c.-236T>G	NP_001305325.1:n.-236T>G