Canonical Allele Identifier: CA1519925028

Gene: KLKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186257404G= , CM000666.2:g.186257404G=	GRCh38
NC_000004.11:g.187178558G= , CM000666.1:g.187178558G=	GRCh37
NC_000004.10:g.187415552G=	NCBI36
NG_012095.2:g.53426G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264690.11:c.1725+39G= MANE Select	ENSP00000264690.6:n.1725+39G=
ENST00000264690.10:c.1725+39G=	ENSP00000264690.6:n.1725+39G=
ENST00000511406.5:n.1786+39G=
ENST00000511608.5:c.1868+39G=
ENST00000513864.2:c.1472-617G=	ENSP00000424469.2:n.1472-617G=
NM_000892.3:c.1725+39G=	NP_000883.2:n.1725+39G=
XM_011531930.1:c.1758+39G=	XP_011530232.1:n.1758+39G=
XM_011531931.1:c.1758+39G=	XP_011530233.1:n.1758+39G=
XM_011531932.1:c.1644+39G=	XP_011530234.1:n.1644+39G=
XM_011531933.1:c.1644+39G=	XP_011530235.1:n.1644+39G=
XM_011531934.1:c.1119+39G=	XP_011530236.1:n.1119+39G=
NM_000892.4:c.1725+39G=	NP_000883.2:n.1725+39G=
NM_001318394.1:c.1472-617G=	NP_001305323.1:n.1472-617G=
NM_001318396.1:c.1119+39G=	NP_001305325.1:n.1119+39G=
XM_011531930.2:c.1758+39G=	XP_011530232.1:n.1758+39G=
XM_017008181.1:c.1758+39G=	XP_016863670.1:n.1758+39G=
XM_017008182.1:c.1619-617G=	XP_016863671.1:n.1619-617G=
XM_017008183.1:c.1586-617G=	XP_016863672.1:n.1586-617G=
XM_017008184.1:c.1119+39G=	XP_016863673.1:n.1119+39G=
NM_000892.5:c.1725+39G= MANE Select	NP_000883.2:n.1725+39G=
NM_001318394.2:c.1472-617G=	NP_001305323.1:n.1472-617G=
NM_001318396.2:c.1119+39G=	NP_001305325.1:n.1119+39G=