Canonical Allele Identifier: CA407025029

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363307C>A (hg19) ; chr19:g.50860051C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860051C>A , CM000681.2:g.50860051C>A	GRCh38
NC_000019.9:g.51363307C>A , CM000681.1:g.51363307C>A	GRCh37
NC_000019.8:g.56055119C>A	NCBI36
NG_011653.1:g.10137C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.710C>A MANE Select	ENSP00000314151.1:p.Pro237His
ENST00000326003.6:c.710C>A	ENSP00000314151.1:p.Pro237His
ENST00000360617.7:c.1152C>A	ENSP00000353829.2:n.1152C>A
ENST00000422986.6:c.*366C>A	ENSP00000393628.2:n.*366C>A
ENST00000595392.5:c.*211C>A	ENSP00000468912.1:n.*211C>A
ENST00000595952.5:c.581C>A	ENSP00000471155.1:p.Pro194His
ENST00000596333.1:n.888C>A
ENST00000598145.1:c.712C>A
ENST00000601349.5:n.1989C>A
ENST00000601812.1:n.1142C>A
ENST00000617027.4:c.587C>A	ENSP00000483513.1:p.Pro196His
NM_001030047.1:c.*435C>A	NP_001025218.1:n.*435C>A
NM_001030048.1:c.581C>A	NP_001025219.1:p.Pro194His
NM_001648.2:c.710C>A MANE Select	NP_001639.1:p.Pro237His
XM_011526923.1:c.728C>A	XP_011525225.1:p.Pro243His
XR_935817.1:n.1324+797C>A