Canonical Allele Identifier: CA309633970

Gene: KLK3

Linked Data

• dbSNP Id: rs963195194
• gnomAD v2: 19-51363335-G-A
• gnomAD v4: 19-50860079-G-A
• MyVariant Identifiers: chr19:g.51363335G>A (hg19) ; chr19:g.50860079G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860079G>A , CM000681.2:g.50860079G>A	GRCh38
NC_000019.9:g.51363335G>A , CM000681.1:g.51363335G>A	GRCh37
NC_000019.8:g.56055147G>A	NCBI36
NG_011653.1:g.10165G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.738G>A MANE Select	ENSP00000314151.1:p.Val246=
ENST00000326003.6:c.738G>A	ENSP00000314151.1:p.Val246=
ENST00000360617.7:c.1180G>A	ENSP00000353829.2:n.1180G>A
ENST00000422986.6:c.*394G>A	ENSP00000393628.2:n.*394G>A
ENST00000595392.5:c.*239G>A	ENSP00000468912.1:n.*239G>A
ENST00000595952.5:c.609G>A	ENSP00000471155.1:p.Val203=
ENST00000596333.1:n.916G>A
ENST00000598145.1:c.740G>A
ENST00000601349.5:n.2017G>A
ENST00000601812.1:n.1170G>A
ENST00000617027.4:c.615G>A	ENSP00000483513.1:p.Val205=
NM_001030047.1:c.*463G>A	NP_001025218.1:n.*463G>A
NM_001030048.1:c.609G>A	NP_001025219.1:p.Val203=
NM_001648.2:c.738G>A MANE Select	NP_001639.1:p.Val246=
XM_011526923.1:c.756G>A	XP_011525225.1:p.Val252=
XR_935817.1:n.1324+825G>A