Canonical Allele Identifier: CA9604614

Gene: KLK3

Linked Data

• dbSNP Id: rs780743219
• ExAC: 19:51363378 C / T
• gnomAD v2: 19-51363378-C-T
• MyVariant Identifiers: chr19:g.51363378C>T (hg19) ; chr19:g.50860122C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.781C>T MANE Select	ENSP00000314151.1:p.Pro261Ser
ENST00000326003.6:c.781C>T	ENSP00000314151.1:p.Pro261Ser
ENST00000360617.7:c.1223C>T	ENSP00000353829.2:n.1223C>T
ENST00000422986.6:c.*437C>T	ENSP00000393628.2:n.*437C>T
ENST00000595392.5:c.*282C>T	ENSP00000468912.1:n.*282C>T
ENST00000595952.5:c.652C>T	ENSP00000471155.1:p.Pro218Ser
ENST00000596333.1:n.959C>T
ENST00000598145.1:c.783C>T
ENST00000601349.5:n.2060C>T
ENST00000601812.1:n.1213C>T
ENST00000617027.4:c.658C>T	ENSP00000483513.1:p.Pro220Ser
NM_001030047.1:c.*506C>T	NP_001025218.1:n.*506C>T
NM_001030048.1:c.652C>T	NP_001025219.1:p.Pro218Ser
NM_001648.2:c.781C>T MANE Select	NP_001639.1:p.Pro261Ser
XM_011526923.1:c.799C>T	XP_011525225.1:p.Pro267Ser
XR_935817.1:n.1324+868C>T