Canonical Allele Identifier: CA407025230

Gene: KLK3

Linked Data

• gnomAD v4: 19-50860112-C-G
• MyVariant Identifiers: chr19:g.51363368C>G (hg19) ; chr19:g.50860112C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860112C>G , CM000681.2:g.50860112C>G	GRCh38
NC_000019.9:g.51363368C>G , CM000681.1:g.51363368C>G	GRCh37
NC_000019.8:g.56055180C>G	NCBI36
NG_011653.1:g.10198C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.771C>G MANE Select	ENSP00000314151.1:p.Ile257Met
ENST00000326003.6:c.771C>G	ENSP00000314151.1:p.Ile257Met
ENST00000360617.7:c.1213C>G	ENSP00000353829.2:n.1213C>G
ENST00000422986.6:c.*427C>G	ENSP00000393628.2:n.*427C>G
ENST00000595392.5:c.*272C>G	ENSP00000468912.1:n.*272C>G
ENST00000595952.5:c.642C>G	ENSP00000471155.1:p.Ile214Met
ENST00000596333.1:n.949C>G
ENST00000598145.1:c.773C>G
ENST00000601349.5:n.2050C>G
ENST00000601812.1:n.1203C>G
ENST00000617027.4:c.648C>G	ENSP00000483513.1:p.Ile216Met
NM_001030047.1:c.*496C>G	NP_001025218.1:n.*496C>G
NM_001030048.1:c.642C>G	NP_001025219.1:p.Ile214Met
NM_001648.2:c.771C>G MANE Select	NP_001639.1:p.Ile257Met
XM_011526923.1:c.789C>G	XP_011525225.1:p.Ile263Met
XR_935817.1:n.1324+858C>G