Canonical Allele Identifier: CA407025151

Gene: KLK3

Linked Data

• gnomAD v4: 19-50860078-T-G
• MyVariant Identifiers: chr19:g.51363334T>G (hg19) ; chr19:g.50860078T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860078T>G , CM000681.2:g.50860078T>G	GRCh38
NC_000019.9:g.51363334T>G , CM000681.1:g.51363334T>G	GRCh37
NC_000019.8:g.56055146T>G	NCBI36
NG_011653.1:g.10164T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.737T>G MANE Select	ENSP00000314151.1:p.Val246Gly
ENST00000326003.6:c.737T>G	ENSP00000314151.1:p.Val246Gly
ENST00000360617.7:c.1179T>G	ENSP00000353829.2:n.1179T>G
ENST00000422986.6:c.*393T>G	ENSP00000393628.2:n.*393T>G
ENST00000595392.5:c.*238T>G	ENSP00000468912.1:n.*238T>G
ENST00000595952.5:c.608T>G	ENSP00000471155.1:p.Val203Gly
ENST00000596333.1:n.915T>G
ENST00000598145.1:c.739T>G
ENST00000601349.5:n.2016T>G
ENST00000601812.1:n.1169T>G
ENST00000617027.4:c.614T>G	ENSP00000483513.1:p.Val205Gly
NM_001030047.1:c.*462T>G	NP_001025218.1:n.*462T>G
NM_001030048.1:c.608T>G	NP_001025219.1:p.Val203Gly
NM_001648.2:c.737T>G MANE Select	NP_001639.1:p.Val246Gly
XM_011526923.1:c.755T>G	XP_011525225.1:p.Val252Gly
XR_935817.1:n.1324+824T>G