Canonical Allele Identifier: CA407025271

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363378C>G (hg19) ; chr19:g.50860122C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860122C>G , CM000681.2:g.50860122C>G	GRCh38
NC_000019.9:g.51363378C>G , CM000681.1:g.51363378C>G	GRCh37
NC_000019.8:g.56055190C>G	NCBI36
NG_011653.1:g.10208C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.781C>G MANE Select	ENSP00000314151.1:p.Pro261Ala
ENST00000326003.6:c.781C>G	ENSP00000314151.1:p.Pro261Ala
ENST00000360617.7:c.1223C>G	ENSP00000353829.2:n.1223C>G
ENST00000422986.6:c.*437C>G	ENSP00000393628.2:n.*437C>G
ENST00000595392.5:c.*282C>G	ENSP00000468912.1:n.*282C>G
ENST00000595952.5:c.652C>G	ENSP00000471155.1:p.Pro218Ala
ENST00000596333.1:n.959C>G
ENST00000598145.1:c.783C>G
ENST00000601349.5:n.2060C>G
ENST00000601812.1:n.1213C>G
ENST00000617027.4:c.658C>G	ENSP00000483513.1:p.Pro220Ala
NM_001030047.1:c.*506C>G	NP_001025218.1:n.*506C>G
NM_001030048.1:c.652C>G	NP_001025219.1:p.Pro218Ala
NM_001648.2:c.781C>G MANE Select	NP_001639.1:p.Pro261Ala
XM_011526923.1:c.799C>G	XP_011525225.1:p.Pro267Ala
XR_935817.1:n.1324+868C>G