Canonical Allele Identifier: CA309633780

Gene: KLK3

Linked Data

• dbSNP Id: rs898593349
• gnomAD v3: 19-50859894-T-C
• gnomAD v4: 19-50859894-T-C
• MyVariant Identifiers: chr19:g.51363150T>C (hg19) ; chr19:g.50859894T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50859894T>C , CM000681.2:g.50859894T>C	GRCh38
NC_000019.9:g.51363150T>C , CM000681.1:g.51363150T>C	GRCh37
NC_000019.8:g.56054962T>C	NCBI36
NG_011653.1:g.9980T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.631-78T>C MANE Select	ENSP00000314151.1:n.631-78T>C
ENST00000326003.6:c.631-78T>C	ENSP00000314151.1:n.631-78T>C
ENST00000360617.7:c.995T>C	ENSP00000353829.2:n.995T>C
ENST00000422986.6:c.*287-78T>C	ENSP00000393628.2:n.*287-78T>C
ENST00000595392.5:c.*132-78T>C	ENSP00000468912.1:n.*132-78T>C
ENST00000595952.5:c.502-78T>C	ENSP00000471155.1:n.502-78T>C
ENST00000596185.5:c.*739-78T>C	ENSP00000471648.1:n.*739-78T>C
ENST00000596333.1:n.809-78T>C
ENST00000598145.1:c.633-78T>C
ENST00000601349.5:n.1910-78T>C
ENST00000601812.1:n.1063-78T>C
ENST00000617027.4:c.508-78T>C	ENSP00000483513.1:n.508-78T>C
NM_001030047.1:c.*278T>C	NP_001025218.1:n.*278T>C
NM_001030048.1:c.502-78T>C	NP_001025219.1:n.502-78T>C
NM_001648.2:c.631-78T>C MANE Select	NP_001639.1:n.631-78T>C
XM_011526923.1:c.649-78T>C	XP_011525225.1:n.649-78T>C
XM_011526924.1:c.*278T>C	XP_011525226.1:n.*278T>C
XR_935817.1:n.1324+640T>C