Canonical Allele Identifier: CA883222159

Gene: KLK3

Linked Data

• dbSNP Id: rs1393715156
• gnomAD v4: 19-50860400-G-T
• MyVariant Identifiers: chr19:g.51363656G>T (hg19) ; chr19:g.50860400G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860400G>T , CM000681.2:g.50860400G>T	GRCh38
NC_000019.9:g.51363656G>T , CM000681.1:g.51363656G>T	GRCh37
NC_000019.8:g.56055468G>T	NCBI36
NG_011653.1:g.10486G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.*273G>T MANE Select	ENSP00000314151.1:n.*273G>T
ENST00000326003.6:c.*273G>T	ENSP00000314151.1:n.*273G>T
ENST00000360617.7:c.1501G>T	ENSP00000353829.2:n.1501G>T
ENST00000422986.6:c.*715G>T	ENSP00000393628.2:n.*715G>T
ENST00000595952.5:c.*273G>T	ENSP00000471155.1:n.*273G>T
ENST00000596333.1:n.1237G>T
ENST00000601349.5:n.2338G>T
ENST00000617027.4:c.*273G>T	ENSP00000483513.1:n.*273G>T
NM_001030047.1:c.*784G>T	NP_001025218.1:n.*784G>T
NM_001030048.1:c.*273G>T	NP_001025219.1:n.*273G>T
NM_001648.2:c.*273G>T MANE Select	NP_001639.1:n.*273G>T
XM_011526923.1:c.*273G>T	XP_011525225.1:n.*273G>T
XR_935817.1:n.1324+1146G>T