Canonical Allele Identifier: CA309634134

Gene: KLK3

Linked Data

• dbSNP Id: rs1141894
• gnomAD v2: 19-51363474-T-C
• gnomAD v3: 19-50860218-T-C
• gnomAD v4: 19-50860218-T-C
• MyVariant Identifiers: chr19:g.51363474T>C (hg19) ; chr19:g.50860218T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860218T>C , CM000681.2:g.50860218T>C	GRCh38
NC_000019.9:g.51363474T>C , CM000681.1:g.51363474T>C	GRCh37
NC_000019.8:g.56055286T>C	NCBI36
NG_011653.1:g.10304T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.*91T>C MANE Select	ENSP00000314151.1:n.*91T>C
ENST00000326003.6:c.*91T>C	ENSP00000314151.1:n.*91T>C
ENST00000360617.7:c.1319T>C	ENSP00000353829.2:n.1319T>C
ENST00000422986.6:c.*533T>C	ENSP00000393628.2:n.*533T>C
ENST00000595392.5:c.*378T>C	ENSP00000468912.1:n.*378T>C
ENST00000595952.5:c.*91T>C	ENSP00000471155.1:n.*91T>C
ENST00000596333.1:n.1055T>C
ENST00000601349.5:n.2156T>C
ENST00000617027.4:c.*91T>C	ENSP00000483513.1:n.*91T>C
NM_001030047.1:c.*602T>C	NP_001025218.1:n.*602T>C
NM_001030048.1:c.*91T>C	NP_001025219.1:n.*91T>C
NM_001648.2:c.*91T>C MANE Select	NP_001639.1:n.*91T>C
XM_011526923.1:c.*91T>C	XP_011525225.1:n.*91T>C
XR_935817.1:n.1324+964T>C