Canonical Allele Identifier: CA883219319

Gene: KLK3

Linked Data

• dbSNP Id: rs1362008948
• gnomAD v3: 19-50856850-C-G
• gnomAD v4: 19-50856850-C-G
• MyVariant Identifiers: chr19:g.51360106C>G (hg19) ; chr19:g.50856850C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50856850C>G , CM000681.2:g.50856850C>G	GRCh38
NC_000019.9:g.51360106C>G , CM000681.1:g.51360106C>G	GRCh37
NC_000019.8:g.56051918C>G	NCBI36
NG_011653.1:g.6936C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.206+451C>G MANE Select	ENSP00000314151.1:n.206+451C>G
ENST00000326003.6:c.206+451C>G	ENSP00000314151.1:n.206+451C>G
ENST00000360617.7:c.206+451C>G	ENSP00000353829.2:n.206+451C>G
ENST00000422986.6:c.206+451C>G	ENSP00000393628.2:n.206+451C>G
ENST00000593997.5:c.206+451C>G	ENSP00000472907.1:n.206+451C>G
ENST00000595392.5:c.206+451C>G	ENSP00000468912.1:n.206+451C>G
ENST00000595952.5:c.206+451C>G	ENSP00000471155.1:n.206+451C>G
ENST00000596185.5:c.*314+451C>G	ENSP00000471648.1:n.*314+451C>G
ENST00000596333.1:n.241+451C>G
ENST00000597286.5:c.95+451C>G	ENSP00000470523.1:n.95+451C>G
ENST00000597483.5:c.206+451C>G	ENSP00000472411.1:n.206+451C>G
ENST00000598145.1:c.190+451C>G
ENST00000601349.5:n.1485+451C>G
ENST00000601503.5:c.149+451C>G	ENSP00000472213.1:n.149+451C>G
ENST00000617027.4:c.206+451C>G	ENSP00000483513.1:n.206+451C>G
NM_001030047.1:c.206+451C>G	NP_001025218.1:n.206+451C>G
NM_001030048.1:c.206+451C>G	NP_001025219.1:n.206+451C>G
NM_001648.2:c.206+451C>G MANE Select	NP_001639.1:n.206+451C>G
XM_011526923.1:c.206+451C>G	XP_011525225.1:n.206+451C>G
XM_011526924.1:c.206+451C>G	XP_011525226.1:n.206+451C>G
XR_935817.1:n.241+451C>G