Canonical Allele Identifier: CA442640325

Gene: KLKB1

Linked Data

• COSMIC: COSM3131132 ; COSM3131133
• MyVariant Identifiers: chr4:g.187158032C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186236878C>A , CM000666.2:g.186236878C>A	GRCh38
NC_000004.11:g.187158032C>A , CM000666.1:g.187158032C>A	GRCh37
NC_000004.10:g.187395026C>A	NCBI36
NG_012095.2:g.32900C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264690.11:c.426C>A MANE Select	ENSP00000264690.6:p.Thr142=
ENST00000264690.10:c.426C>A	ENSP00000264690.6:p.Thr142=
ENST00000428196.5:c.426C>A	ENSP00000412366.1:p.Thr142=
ENST00000446598.6:c.312C>A	ENSP00000415563.2:p.Thr104=
ENST00000511406.5:n.456C>A
ENST00000511608.5:c.569C>A
ENST00000513864.2:c.312C>A	ENSP00000424469.2:p.Thr104=
NM_000892.3:c.426C>A	NP_000883.2:p.Thr142=
XM_011531930.1:c.426C>A	XP_011530232.1:p.Thr142=
XM_011531931.1:c.426C>A	XP_011530233.1:p.Thr142=
XM_011531932.1:c.312C>A	XP_011530234.1:p.Thr104=
XM_011531933.1:c.312C>A	XP_011530235.1:p.Thr104=
XM_011531934.1:c.-212C>A	XP_011530236.1:n.-212C>A
NM_000892.4:c.426C>A	NP_000883.2:p.Thr142=
NM_001318394.1:c.312C>A	NP_001305323.1:p.Thr104=
NM_001318396.1:c.-212C>A	NP_001305325.1:n.-212C>A
XM_011531930.2:c.426C>A	XP_011530232.1:p.Thr142=
XM_017008181.1:c.426C>A	XP_016863670.1:p.Thr142=
XM_017008182.1:c.426C>A	XP_016863671.1:p.Thr142=
XM_017008183.1:c.426C>A	XP_016863672.1:p.Thr142=
NM_000892.5:c.426C>A MANE Select	NP_000883.2:p.Thr142=
NM_001318394.2:c.312C>A	NP_001305323.1:p.Thr104=
NM_001318396.2:c.-212C>A	NP_001305325.1:n.-212C>A