Canonical Allele Identifier: CA1519922539

Gene: KLKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186252131G= , CM000666.2:g.186252131G=	GRCh38
NC_000004.11:g.187173285G= , CM000666.1:g.187173285G=	GRCh37
NC_000004.10:g.187410279G=	NCBI36
NG_012095.2:g.48153G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000892.5:c.1259G= MANE Select	NP_000883.2:p.Gly420=
ENST00000264690.11:c.1259G= MANE Select	ENSP00000264690.6:p.Gly420=
NM_000892.3:c.1259G=	NP_000883.2:p.Gly420=
NM_000892.4:c.1259G=	NP_000883.2:p.Gly420=
NM_001318394.1:c.1145G=	NP_001305323.1:p.Gly382=
NM_001318394.2:c.1145G=	NP_001305323.1:p.Gly382=
NM_001318396.1:c.653G=	NP_001305325.1:p.Gly218=
NM_001318396.2:c.653G=	NP_001305325.1:p.Gly218=
ENST00000264690.10:c.1259G=	ENSP00000264690.6:p.Gly420=
ENST00000467271.1:n.688G=
ENST00000511406.5:n.1320G=
ENST00000511608.5:c.1402G=
ENST00000513864.2:c.1145G=	ENSP00000424469.2:p.Gly382=
XM_011531930.1:c.1292G=	XP_011530232.1:p.Gly431=
XM_011531930.2:c.1292G=	XP_011530232.1:p.Gly431=
XM_011531931.1:c.1292G=	XP_011530233.1:p.Gly431=
XM_011531932.1:c.1178G=	XP_011530234.1:p.Gly393=
XM_011531933.1:c.1178G=	XP_011530235.1:p.Gly393=
XM_011531934.1:c.653G=	XP_011530236.1:p.Gly218=
XM_017008181.1:c.1292G=	XP_016863670.1:p.Gly431=
XM_017008182.1:c.1292G=	XP_016863671.1:p.Gly431=
XM_017008183.1:c.1259G=	XP_016863672.1:p.Gly420=
XM_017008184.1:c.653G=	XP_016863673.1:p.Gly218=