Canonical Allele Identifier: CA2341124650

Gene: KLK2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50878521C= , CM000681.2:g.50878521C=	GRCh38
NC_000019.9:g.51381777C= , CM000681.1:g.51381777C=	GRCh37
NC_000019.8:g.56073589C=	NCBI36
NG_031984.1:g.10089C=

Transcript Alleles

HGVS	Amino-acid Change
NM_005551.5:c.748C= MANE Select	NP_005542.1:p.Arg250=
ENST00000325321.8:c.748C= MANE Select	ENSP00000313581.2:p.Arg250=
NM_001002231.2:c.*113C=	NP_001002231.1:n.*113C=
NM_001002231.3:c.*113C=	NP_001002231.1:n.*113C=
NM_001256080.1:c.442C=	NP_001243009.1:p.Arg148=
NM_001256080.2:c.442C=	NP_001243009.1:p.Arg148=
NM_005551.4:c.748C=	NP_005542.1:p.Arg250=
NR_045762.1:n.813C=
NR_045762.2:n.807C=
NR_045763.1:n.875C=
NR_045763.2:n.869C=
ENST00000325321.7:c.748C=	ENSP00000313581.2:p.Arg250=
ENST00000358049.8:c.*113C=	ENSP00000350748.3:n.*113C=
ENST00000391810.6:c.442C=	ENSP00000375686.2:p.Arg148=
ENST00000594174.5:c.*624C=	ENSP00000472095.1:n.*624C=
ENST00000595050.1:c.466C=
ENST00000595173.1:n.983C=
ENST00000597439.1:c.*277C=	ENSP00000471214.1:n.*277C=
ENST00000597461.1:n.431C=
ENST00000597911.1:c.327C=
ENST00000599121.5:c.*438C=	ENSP00000472499.1:n.*438C=
ENST00000600755.5:n.890C=
ENST00000600866.1:n.730C=
XM_006723206.1:c.835C=	XP_006723269.1:p.Arg279=
XM_006723208.1:c.529C=	XP_006723271.1:p.Arg177=
XM_011526943.1:c.843C=	XP_011525245.1:p.Thr281=
XM_011526944.1:c.798C=	XP_011525246.1:p.Thr266=
XM_011526949.1:c.537C=	XP_011525251.1:p.Thr179=