Canonical Allele Identifier: CA309634299

Gene: KLK3

Linked Data

• dbSNP Id: rs537315899
• gnomAD v2: 19-51363686-T-G
• gnomAD v3: 19-50860430-T-G
• gnomAD v4: 19-50860430-T-G
• MyVariant Identifiers: chr19:g.51363686T>G (hg19) ; chr19:g.50860430T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860430T>G , CM000681.2:g.50860430T>G	GRCh38
NC_000019.9:g.51363686T>G , CM000681.1:g.51363686T>G	GRCh37
NC_000019.8:g.56055498T>G	NCBI36
NG_011653.1:g.10516T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.*303T>G MANE Select	ENSP00000314151.1:n.*303T>G
ENST00000326003.6:c.*303T>G	ENSP00000314151.1:n.*303T>G
ENST00000360617.7:c.1531T>G	ENSP00000353829.2:n.1531T>G
ENST00000422986.6:c.*745T>G	ENSP00000393628.2:n.*745T>G
ENST00000595952.5:c.*303T>G	ENSP00000471155.1:n.*303T>G
ENST00000596333.1:n.1267T>G
ENST00000601349.5:n.2368T>G
ENST00000617027.4:c.*303T>G	ENSP00000483513.1:n.*303T>G
NM_001030047.1:c.*814T>G	NP_001025218.1:n.*814T>G
NM_001030048.1:c.*303T>G	NP_001025219.1:n.*303T>G
NM_001648.2:c.*303T>G MANE Select	NP_001639.1:n.*303T>G
XM_011526923.1:c.*303T>G	XP_011525225.1:n.*303T>G
XR_935817.1:n.1324+1176T>G