Canonical Allele Identifier: CA358945235

Gene: KLKB1

Linked Data

• dbSNP Id: rs1361582656
• gnomAD v2: 4-187158025-G-T
• gnomAD v4: 4-186236871-G-T
• MyVariant Identifiers: chr4:g.187158025G>T (hg19) ; chr4:g.186236871G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186236871G>T , CM000666.2:g.186236871G>T	GRCh38
NC_000004.11:g.187158025G>T , CM000666.1:g.187158025G>T	GRCh37
NC_000004.10:g.187395019G>T	NCBI36
NG_012095.2:g.32893G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264690.11:c.419G>T MANE Select	ENSP00000264690.6:p.Arg140Met
ENST00000264690.10:c.419G>T	ENSP00000264690.6:p.Arg140Met
ENST00000428196.5:c.419G>T	ENSP00000412366.1:p.Arg140Met
ENST00000446598.6:c.305G>T	ENSP00000415563.2:p.Arg102Met
ENST00000511406.5:n.449G>T
ENST00000511608.5:c.562G>T
ENST00000513864.2:c.305G>T	ENSP00000424469.2:p.Arg102Met
NM_000892.3:c.419G>T	NP_000883.2:p.Arg140Met
XM_011531930.1:c.419G>T	XP_011530232.1:p.Arg140Met
XM_011531931.1:c.419G>T	XP_011530233.1:p.Arg140Met
XM_011531932.1:c.305G>T	XP_011530234.1:p.Arg102Met
XM_011531933.1:c.305G>T	XP_011530235.1:p.Arg102Met
XM_011531934.1:c.-219G>T	XP_011530236.1:n.-219G>T
NM_000892.4:c.419G>T	NP_000883.2:p.Arg140Met
NM_001318394.1:c.305G>T	NP_001305323.1:p.Arg102Met
NM_001318396.1:c.-219G>T	NP_001305325.1:n.-219G>T
XM_011531930.2:c.419G>T	XP_011530232.1:p.Arg140Met
XM_017008181.1:c.419G>T	XP_016863670.1:p.Arg140Met
XM_017008182.1:c.419G>T	XP_016863671.1:p.Arg140Met
XM_017008183.1:c.419G>T	XP_016863672.1:p.Arg140Met
NM_000892.5:c.419G>T MANE Select	NP_000883.2:p.Arg140Met
NM_001318394.2:c.305G>T	NP_001305323.1:p.Arg102Met
NM_001318396.2:c.-219G>T	NP_001305325.1:n.-219G>T