Canonical Allele Identifier: CA442643889

Gene: KLKB1

Linked Data

• MyVariant Identifiers: chr4:g.187178489C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186257335C>A , CM000666.2:g.186257335C>A	GRCh38
NC_000004.11:g.187178489C>A , CM000666.1:g.187178489C>A	GRCh37
NC_000004.10:g.187415483C>A	NCBI36
NG_012095.2:g.53357C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264690.11:c.1695C>A MANE Select	ENSP00000264690.6:p.Gly565=
ENST00000264690.10:c.1695C>A	ENSP00000264690.6:p.Gly565=
ENST00000511406.5:n.1756C>A
ENST00000511608.5:c.1838C>A
ENST00000513864.2:c.1472-686C>A	ENSP00000424469.2:n.1472-686C>A
NM_000892.3:c.1695C>A	NP_000883.2:p.Gly565=
XM_011531930.1:c.1728C>A	XP_011530232.1:p.Gly576=
XM_011531931.1:c.1728C>A	XP_011530233.1:p.Gly576=
XM_011531932.1:c.1614C>A	XP_011530234.1:p.Gly538=
XM_011531933.1:c.1614C>A	XP_011530235.1:p.Gly538=
XM_011531934.1:c.1089C>A	XP_011530236.1:p.Gly363=
NM_000892.4:c.1695C>A	NP_000883.2:p.Gly565=
NM_001318394.1:c.1472-686C>A	NP_001305323.1:n.1472-686C>A
NM_001318396.1:c.1089C>A	NP_001305325.1:p.Gly363=
XM_011531930.2:c.1728C>A	XP_011530232.1:p.Gly576=
XM_017008181.1:c.1728C>A	XP_016863670.1:p.Gly576=
XM_017008182.1:c.1619-686C>A	XP_016863671.1:n.1619-686C>A
XM_017008183.1:c.1586-686C>A	XP_016863672.1:n.1586-686C>A
XM_017008184.1:c.1089C>A	XP_016863673.1:p.Gly363=
NM_000892.5:c.1695C>A MANE Select	NP_000883.2:p.Gly565=
NM_001318394.2:c.1472-686C>A	NP_001305323.1:n.1472-686C>A
NM_001318396.2:c.1089C>A	NP_001305325.1:p.Gly363=