Canonical Allele Identifier: CA407024993

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363298G>C (hg19) ; chr19:g.50860042G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860042G>C , CM000681.2:g.50860042G>C	GRCh38
NC_000019.9:g.51363298G>C , CM000681.1:g.51363298G>C	GRCh37
NC_000019.8:g.56055110G>C	NCBI36
NG_011653.1:g.10128G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.701G>C MANE Select	ENSP00000314151.1:p.Cys234Ser
ENST00000326003.6:c.701G>C	ENSP00000314151.1:p.Cys234Ser
ENST00000360617.7:c.1143G>C	ENSP00000353829.2:n.1143G>C
ENST00000422986.6:c.*357G>C	ENSP00000393628.2:n.*357G>C
ENST00000595392.5:c.*202G>C	ENSP00000468912.1:n.*202G>C
ENST00000595952.5:c.572G>C	ENSP00000471155.1:p.Cys191Ser
ENST00000596333.1:n.879G>C
ENST00000598145.1:c.703G>C
ENST00000601349.5:n.1980G>C
ENST00000601812.1:n.1133G>C
ENST00000617027.4:c.578G>C	ENSP00000483513.1:p.Cys193Ser
NM_001030047.1:c.*426G>C	NP_001025218.1:n.*426G>C
NM_001030048.1:c.572G>C	NP_001025219.1:p.Cys191Ser
NM_001648.2:c.701G>C MANE Select	NP_001639.1:p.Cys234Ser
XM_011526923.1:c.719G>C	XP_011525225.1:p.Cys240Ser
XR_935817.1:n.1324+788G>C