Canonical Allele Identifier: CA407025185

Gene: KLK3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.755G>T MANE Select	ENSP00000314151.1:p.Trp252Leu
ENST00000326003.6:c.755G>T	ENSP00000314151.1:p.Trp252Leu
ENST00000360617.7:c.1197G>T	ENSP00000353829.2:n.1197G>T
ENST00000422986.6:c.*411G>T	ENSP00000393628.2:n.*411G>T
ENST00000595392.5:c.*256G>T	ENSP00000468912.1:n.*256G>T
ENST00000595952.5:c.626G>T	ENSP00000471155.1:p.Trp209Leu
ENST00000596333.1:n.933G>T
ENST00000598145.1:c.757G>T
ENST00000601349.5:n.2034G>T
ENST00000601812.1:n.1187G>T
ENST00000617027.4:c.632G>T	ENSP00000483513.1:p.Trp211Leu
NM_001030047.1:c.*480G>T	NP_001025218.1:n.*480G>T
NM_001030048.1:c.626G>T	NP_001025219.1:p.Trp209Leu
NM_001648.2:c.755G>T MANE Select	NP_001639.1:p.Trp252Leu
XM_011526923.1:c.773G>T	XP_011525225.1:p.Trp258Leu
XR_935817.1:n.1324+842G>T