Canonical Allele Identifier: CA358944967

Gene: KLKB1

Linked Data

• MyVariant Identifiers: chr4:g.187157983T>C (hg19) ; chr4:g.186236829T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186236829T>C , CM000666.2:g.186236829T>C	GRCh38
NC_000004.11:g.187157983T>C , CM000666.1:g.187157983T>C	GRCh37
NC_000004.10:g.187394977T>C	NCBI36
NG_012095.2:g.32851T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264690.11:c.377T>C MANE Select	ENSP00000264690.6:p.Phe126Ser
ENST00000264690.10:c.377T>C	ENSP00000264690.6:p.Phe126Ser
ENST00000428196.5:c.377T>C	ENSP00000412366.1:p.Phe126Ser
ENST00000446598.6:c.263T>C	ENSP00000415563.2:p.Phe88Ser
ENST00000511406.5:n.407T>C
ENST00000511608.5:c.520T>C
ENST00000513864.2:c.263T>C	ENSP00000424469.2:p.Phe88Ser
NM_000892.3:c.377T>C	NP_000883.2:p.Phe126Ser
XM_011531930.1:c.377T>C	XP_011530232.1:p.Phe126Ser
XM_011531931.1:c.377T>C	XP_011530233.1:p.Phe126Ser
XM_011531932.1:c.263T>C	XP_011530234.1:p.Phe88Ser
XM_011531933.1:c.263T>C	XP_011530235.1:p.Phe88Ser
XM_011531934.1:c.-261T>C	XP_011530236.1:n.-261T>C
NM_000892.4:c.377T>C	NP_000883.2:p.Phe126Ser
NM_001318394.1:c.263T>C	NP_001305323.1:p.Phe88Ser
NM_001318396.1:c.-261T>C	NP_001305325.1:n.-261T>C
XM_011531930.2:c.377T>C	XP_011530232.1:p.Phe126Ser
XM_017008181.1:c.377T>C	XP_016863670.1:p.Phe126Ser
XM_017008182.1:c.377T>C	XP_016863671.1:p.Phe126Ser
XM_017008183.1:c.377T>C	XP_016863672.1:p.Phe126Ser
NM_000892.5:c.377T>C MANE Select	NP_000883.2:p.Phe126Ser
NM_001318394.2:c.263T>C	NP_001305323.1:p.Phe88Ser
NM_001318396.2:c.-261T>C	NP_001305325.1:n.-261T>C