Canonical Allele Identifier: CA309634355

Gene: KLK3

Linked Data

• dbSNP Id: rs752217318
• gnomAD v2: 19-51363715-T-C
• gnomAD v3: 19-50860459-T-C
• gnomAD v4: 19-50860459-T-C
• MyVariant Identifiers: chr19:g.51363715T>C (hg19) ; chr19:g.50860459T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860459T>C , CM000681.2:g.50860459T>C	GRCh38
NC_000019.9:g.51363715T>C , CM000681.1:g.51363715T>C	GRCh37
NC_000019.8:g.56055527T>C	NCBI36
NG_011653.1:g.10545T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.*332T>C MANE Select	ENSP00000314151.1:n.*332T>C
ENST00000326003.6:c.*332T>C	ENSP00000314151.1:n.*332T>C
ENST00000360617.7:c.1560T>C	ENSP00000353829.2:n.1560T>C
ENST00000422986.6:c.*774T>C	ENSP00000393628.2:n.*774T>C
ENST00000596333.1:n.1296T>C
ENST00000601349.5:n.2397T>C
ENST00000617027.4:c.*332T>C	ENSP00000483513.1:n.*332T>C
NM_001030047.1:c.*843T>C	NP_001025218.1:n.*843T>C
NM_001030048.1:c.*332T>C	NP_001025219.1:n.*332T>C
NM_001648.2:c.*332T>C MANE Select	NP_001639.1:n.*332T>C
XM_011526923.1:c.*332T>C	XP_011525225.1:n.*332T>C
XR_935817.1:n.1324+1205T>C