Canonical Allele Identifier: CA633899601

Gene: KLK3

Linked Data

• dbSNP Id: rs1436539959
• gnomAD v2: 19-51363421-C-A
• gnomAD v4: 19-50860165-C-A
• MyVariant Identifiers: chr19:g.51363421C>A (hg19) ; chr19:g.50860165C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860165C>A , CM000681.2:g.50860165C>A	GRCh38
NC_000019.9:g.51363421C>A , CM000681.1:g.51363421C>A	GRCh37
NC_000019.8:g.56055233C>A	NCBI36
NG_011653.1:g.10251C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.*38C>A MANE Select	ENSP00000314151.1:n.*38C>A
ENST00000326003.6:c.*38C>A	ENSP00000314151.1:n.*38C>A
ENST00000360617.7:c.1266C>A	ENSP00000353829.2:n.1266C>A
ENST00000422986.6:c.*480C>A	ENSP00000393628.2:n.*480C>A
ENST00000595392.5:c.*325C>A	ENSP00000468912.1:n.*325C>A
ENST00000595952.5:c.*38C>A	ENSP00000471155.1:n.*38C>A
ENST00000596333.1:n.1002C>A
ENST00000598145.1:c.826C>A
ENST00000601349.5:n.2103C>A
ENST00000617027.4:c.*38C>A	ENSP00000483513.1:n.*38C>A
NM_001030047.1:c.*549C>A	NP_001025218.1:n.*549C>A
NM_001030048.1:c.*38C>A	NP_001025219.1:n.*38C>A
NM_001648.2:c.*38C>A MANE Select	NP_001639.1:n.*38C>A
XM_011526923.1:c.*38C>A	XP_011525225.1:n.*38C>A
XR_935817.1:n.1324+911C>A