Canonical Allele Identifier: CA309651090

Gene: KLK2

Linked Data

• dbSNP Id: rs906226034
• gnomAD v3: 19-50879752-T-C
• gnomAD v4: 19-50879752-T-C
• MyVariant Identifiers: chr19:g.51383008T>C (hg19) ; chr19:g.50879752T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50879752T>C , CM000681.2:g.50879752T>C	GRCh38
NC_000019.9:g.51383008T>C , CM000681.1:g.51383008T>C	GRCh37
NC_000019.8:g.56074820T>C	NCBI36
NG_031984.1:g.11320T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325321.8:c.*1193T>C MANE Select	ENSP00000313581.2:n.*1193T>C
ENST00000325321.7:c.*1193T>C	ENSP00000313581.2:n.*1193T>C
ENST00000358049.8:c.*1344T>C	ENSP00000350748.3:n.*1344T>C
ENST00000391810.6:c.*1193T>C	ENSP00000375686.2:n.*1193T>C
ENST00000597439.1:c.*1508T>C	ENSP00000471214.1:n.*1508T>C
NM_001002231.2:c.*1344T>C	NP_001002231.1:n.*1344T>C
NM_001256080.1:c.*1193T>C	NP_001243009.1:n.*1193T>C
NM_005551.4:c.*1193T>C	NP_005542.1:n.*1193T>C
NR_045762.1:n.2044T>C
NR_045763.1:n.2106T>C
NM_005551.5:c.*1193T>C MANE Select	NP_005542.1:n.*1193T>C
NM_001002231.3:c.*1344T>C	NP_001002231.1:n.*1344T>C
NR_045762.2:n.2038T>C
NR_045763.2:n.2100T>C
NM_001256080.2:c.*1193T>C	NP_001243009.1:n.*1193T>C