Canonical Allele Identifier: CA2507200500

Gene: KLK2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50879848A>T , CM000681.2:g.50879848A>T	GRCh38
NC_000019.9:g.51383104A>T , CM000681.1:g.51383104A>T	GRCh37
NC_000019.8:g.56074916A>T	NCBI36
NG_031984.1:g.11416A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325321.8:c.*1289A>T MANE Select	ENSP00000313581.2:n.*1289A>T
ENST00000325321.7:c.*1289A>T	ENSP00000313581.2:n.*1289A>T
ENST00000358049.8:c.*1440A>T	ENSP00000350748.3:n.*1440A>T
ENST00000391810.6:c.*1289A>T	ENSP00000375686.2:n.*1289A>T
ENST00000597439.1:c.*1604A>T	ENSP00000471214.1:n.*1604A>T
NM_001002231.2:c.*1440A>T	NP_001002231.1:n.*1440A>T
NM_001256080.1:c.*1289A>T	NP_001243009.1:n.*1289A>T
NM_005551.4:c.*1289A>T	NP_005542.1:n.*1289A>T
NR_045762.1:n.2140A>T
NR_045763.1:n.2202A>T
NM_005551.5:c.*1289A>T MANE Select	NP_005542.1:n.*1289A>T
NM_001002231.3:c.*1440A>T	NP_001002231.1:n.*1440A>T
NR_045762.2:n.2134A>T
NR_045763.2:n.2196A>T
NM_001256080.2:c.*1289A>T	NP_001243009.1:n.*1289A>T