Canonical Allele Identifier: CA407025026

Gene: KLK3

Linked Data

• gnomAD v4: 19-50860050-C-T
• MyVariant Identifiers: chr19:g.51363306C>T (hg19) ; chr19:g.50860050C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860050C>T , CM000681.2:g.50860050C>T	GRCh38
NC_000019.9:g.51363306C>T , CM000681.1:g.51363306C>T	GRCh37
NC_000019.8:g.56055118C>T	NCBI36
NG_011653.1:g.10136C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.709C>T MANE Select	ENSP00000314151.1:p.Pro237Ser
ENST00000326003.6:c.709C>T	ENSP00000314151.1:p.Pro237Ser
ENST00000360617.7:c.1151C>T	ENSP00000353829.2:n.1151C>T
ENST00000422986.6:c.*365C>T	ENSP00000393628.2:n.*365C>T
ENST00000595392.5:c.*210C>T	ENSP00000468912.1:n.*210C>T
ENST00000595952.5:c.580C>T	ENSP00000471155.1:p.Pro194Ser
ENST00000596333.1:n.887C>T
ENST00000598145.1:c.711C>T
ENST00000601349.5:n.1988C>T
ENST00000601812.1:n.1141C>T
ENST00000617027.4:c.586C>T	ENSP00000483513.1:p.Pro196Ser
NM_001030047.1:c.*434C>T	NP_001025218.1:n.*434C>T
NM_001030048.1:c.580C>T	NP_001025219.1:p.Pro194Ser
NM_001648.2:c.709C>T MANE Select	NP_001639.1:p.Pro237Ser
XM_011526923.1:c.727C>T	XP_011525225.1:p.Pro243Ser
XR_935817.1:n.1324+796C>T