Canonical Allele Identifier: CA2341125248
Gene: KLK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50879818C= , CM000681.2:g.50879818C= GRCh38
NC_000019.9:g.51383074C= , CM000681.1:g.51383074C= GRCh37
NC_000019.8:g.56074886C= NCBI36
NG_031984.1:g.11386C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325321.8:c.*1259C= MANE Select ENSP00000313581.2:n.*1259C=
ENST00000325321.7:c.*1259C= ENSP00000313581.2:n.*1259C=
ENST00000358049.8:c.*1410C= ENSP00000350748.3:n.*1410C=
ENST00000391810.6:c.*1259C= ENSP00000375686.2:n.*1259C=
ENST00000597439.1:c.*1574C= ENSP00000471214.1:n.*1574C=
NM_001002231.2:c.*1410C= NP_001002231.1:n.*1410C=
NM_001256080.1:c.*1259C= NP_001243009.1:n.*1259C=
NM_005551.4:c.*1259C= NP_005542.1:n.*1259C=
NR_045762.1:n.2110C=
NR_045763.1:n.2172C=
NM_005551.5:c.*1259C= MANE Select NP_005542.1:n.*1259C=
NM_001002231.3:c.*1410C= NP_001002231.1:n.*1410C=
NR_045762.2:n.2104C=
NR_045763.2:n.2166C=
NM_001256080.2:c.*1259C= NP_001243009.1:n.*1259C=