Canonical Allele Identifier: CA407025186

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363352G>C (hg19) ; chr19:g.50860096G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860096G>C , CM000681.2:g.50860096G>C	GRCh38
NC_000019.9:g.51363352G>C , CM000681.1:g.51363352G>C	GRCh37
NC_000019.8:g.56055164G>C	NCBI36
NG_011653.1:g.10182G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.755G>C MANE Select	ENSP00000314151.1:p.Trp252Ser
ENST00000326003.6:c.755G>C	ENSP00000314151.1:p.Trp252Ser
ENST00000360617.7:c.1197G>C	ENSP00000353829.2:n.1197G>C
ENST00000422986.6:c.*411G>C	ENSP00000393628.2:n.*411G>C
ENST00000595392.5:c.*256G>C	ENSP00000468912.1:n.*256G>C
ENST00000595952.5:c.626G>C	ENSP00000471155.1:p.Trp209Ser
ENST00000596333.1:n.933G>C
ENST00000598145.1:c.757G>C
ENST00000601349.5:n.2034G>C
ENST00000601812.1:n.1187G>C
ENST00000617027.4:c.632G>C	ENSP00000483513.1:p.Trp211Ser
NM_001030047.1:c.*480G>C	NP_001025218.1:n.*480G>C
NM_001030048.1:c.626G>C	NP_001025219.1:p.Trp209Ser
NM_001648.2:c.755G>C MANE Select	NP_001639.1:p.Trp252Ser
XM_011526923.1:c.773G>C	XP_011525225.1:p.Trp258Ser
XR_935817.1:n.1324+842G>C