Canonical Allele Identifier: CA15957736

Gene: KLK2 KLK3

Linked Data

• dbSNP Id: rs2664156
• gnomAD v2: 19-51377163-T-C
• gnomAD v3: 19-50873907-T-C
• gnomAD v4: 19-50873907-T-C
• MyVariant Identifiers: chr19:g.51377163T>C (hg19) ; chr19:g.50873907T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50873907T>C , CM000681.2:g.50873907T>C	GRCh38
NC_000019.9:g.51377163T>C , CM000681.1:g.51377163T>C	GRCh37
NC_000019.8:g.56068975T>C	NCBI36
NG_031984.1:g.5475T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000325321.8:c.46+388T>C (KLK2) MANE Select	ENSP00000313581.2:n.46+388T>C
ENST00000325321.7:c.46+388T>C (KLK2)	ENSP00000313581.2:n.46+388T>C
ENST00000358049.8:c.46+388T>C (KLK2)	ENSP00000350748.3:n.46+388T>C
ENST00000391810.6:c.-101+388T>C (KLK2)	ENSP00000375686.2:n.-101+388T>C
ENST00000593493.5:c.-261+653T>C (KLK2)	ENSP00000472852.1:n.-261+653T>C
ENST00000594174.5:c.46+388T>C (KLK2)	ENSP00000472095.1:n.46+388T>C
ENST00000595316.5:c.46+388T>C (KLK2)	ENSP00000469770.1:n.46+388T>C
ENST00000595375.5:n.221+653T>C (KLK2)
ENST00000596950.5:n.185+653T>C (KLK2)
ENST00000597439.1:c.46+388T>C (KLK2)	ENSP00000471214.1:n.46+388T>C
ENST00000597509.5:n.315+653T>C (KLK2)
ENST00000597727.5:c.46+388T>C (KLK2)	ENSP00000471014.1:n.46+388T>C
ENST00000599121.5:c.46+388T>C (KLK2)	ENSP00000472499.1:n.46+388T>C
ENST00000599280.5:n.87+388T>C (KLK2)
ENST00000600690.5:c.46+388T>C (KLK2)	ENSP00000469318.1:n.46+388T>C
ENST00000600755.5:n.75+388T>C (KLK2)
ENST00000600866.1:n.75+388T>C (KLK2)
ENST00000601743.1:n.434T>C (KLK2)
NM_001002231.2:c.46+388T>C (KLK2)	NP_001002231.1:n.46+388T>C
NM_001256080.1:c.-101+388T>C (KLK2)	NP_001243009.1:n.-101+388T>C
NM_005551.4:c.46+388T>C (KLK2)	NP_005542.1:n.46+388T>C
NR_045762.1:n.87+388T>C (KLK2)
NR_045763.1:n.87+388T>C (KLK2)
XM_006723206.1:c.46+388T>C (KLK2)	XP_006723269.1:n.46+388T>C
XM_006723208.1:c.-101+388T>C (KLK2)	XP_006723271.1:n.-101+388T>C
XM_006723209.2:c.46+388T>C (KLK2)	XP_006723272.1:n.46+388T>C
XM_011526943.1:c.46+388T>C (KLK2)	XP_011525245.1:n.46+388T>C
XM_011526944.1:c.46+388T>C (KLK2)	XP_011525246.1:n.46+388T>C
XM_011526945.1:c.46+388T>C (KLK2)	XP_011525247.1:n.46+388T>C
XM_011526946.1:c.46+388T>C (KLK2)	XP_011525248.1:n.46+388T>C
XM_011526947.1:c.46+388T>C (KLK2)	XP_011525249.1:n.46+388T>C
XM_011526948.1:c.46+388T>C (KLK2)	XP_011525250.1:n.46+388T>C
XM_011526949.1:c.-101+388T>C (KLK2)	XP_011525251.1:n.-101+388T>C
XR_935817.1:n.1325-3774T>C (KLK3)
XR_935824.1:n.87+388T>C (KLK2)
NM_005551.5:c.46+388T>C (KLK2) MANE Select	NP_005542.1:n.46+388T>C
NM_001002231.3:c.46+388T>C (KLK2)	NP_001002231.1:n.46+388T>C
NR_045762.2:n.81+388T>C (KLK2)
NR_045763.2:n.81+388T>C (KLK2)
NM_001256080.2:c.-101+388T>C (KLK2)	NP_001243009.1:n.-101+388T>C