Canonical Allele Identifier: CA309634225

Gene: KLK3

Linked Data

• dbSNP Id: rs958771650
• gnomAD v3: 19-50860350-T-C
• gnomAD v4: 19-50860350-T-C
• MyVariant Identifiers: chr19:g.51363606T>C (hg19) ; chr19:g.50860350T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860350T>C , CM000681.2:g.50860350T>C	GRCh38
NC_000019.9:g.51363606T>C , CM000681.1:g.51363606T>C	GRCh37
NC_000019.8:g.56055418T>C	NCBI36
NG_011653.1:g.10436T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.*223T>C MANE Select	ENSP00000314151.1:n.*223T>C
ENST00000326003.6:c.*223T>C	ENSP00000314151.1:n.*223T>C
ENST00000360617.7:c.1451T>C	ENSP00000353829.2:n.1451T>C
ENST00000422986.6:c.*665T>C	ENSP00000393628.2:n.*665T>C
ENST00000595952.5:c.*223T>C	ENSP00000471155.1:n.*223T>C
ENST00000596333.1:n.1187T>C
ENST00000601349.5:n.2288T>C
ENST00000617027.4:c.*223T>C	ENSP00000483513.1:n.*223T>C
NM_001030047.1:c.*734T>C	NP_001025218.1:n.*734T>C
NM_001030048.1:c.*223T>C	NP_001025219.1:n.*223T>C
NM_001648.2:c.*223T>C MANE Select	NP_001639.1:n.*223T>C
XM_011526923.1:c.*223T>C	XP_011525225.1:n.*223T>C
XR_935817.1:n.1324+1096T>C