Canonical Allele Identifier: CA1519908124

Gene: KLKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186239966G= , CM000666.2:g.186239966G=	GRCh38
NC_000004.11:g.187161120G= , CM000666.1:g.187161120G=	GRCh37
NC_000004.10:g.187398114G=	NCBI36
NG_012095.2:g.35988G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000892.5:c.598+1601G= MANE Select	NP_000883.2:n.598+1601G=
ENST00000264690.11:c.598+1601G= MANE Select	ENSP00000264690.6:n.598+1601G=
NM_000892.3:c.598+1601G=	NP_000883.2:n.598+1601G=
NM_000892.4:c.598+1601G=	NP_000883.2:n.598+1601G=
NM_001318394.1:c.484+1601G=	NP_001305323.1:n.484+1601G=
NM_001318394.2:c.484+1601G=	NP_001305323.1:n.484+1601G=
NM_001318396.1:c.-40+1601G=	NP_001305325.1:n.-40+1601G=
NM_001318396.2:c.-40+1601G=	NP_001305325.1:n.-40+1601G=
ENST00000264690.10:c.598+1601G=	ENSP00000264690.6:n.598+1601G=
ENST00000511406.5:n.628+1601G=
ENST00000511608.5:c.741+1601G=
ENST00000513864.2:c.484+1601G=	ENSP00000424469.2:n.484+1601G=
XM_011531930.1:c.631+1568G=	XP_011530232.1:n.631+1568G=
XM_011531930.2:c.631+1568G=	XP_011530232.1:n.631+1568G=
XM_011531931.1:c.631+1568G=	XP_011530233.1:n.631+1568G=
XM_011531932.1:c.517+1568G=	XP_011530234.1:n.517+1568G=
XM_011531933.1:c.517+1568G=	XP_011530235.1:n.517+1568G=
XM_011531934.1:c.-40+1601G=	XP_011530236.1:n.-40+1601G=
XM_017008181.1:c.631+1568G=	XP_016863670.1:n.631+1568G=
XM_017008182.1:c.631+1568G=	XP_016863671.1:n.631+1568G=
XM_017008183.1:c.598+1601G=	XP_016863672.1:n.598+1601G=
XM_017008184.1:c.-40+1568G=	XP_016863673.1:n.-40+1568G=