Canonical Allele Identifier: CA407025163

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363341T>G (hg19) ; chr19:g.50860085T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860085T>G , CM000681.2:g.50860085T>G	GRCh38
NC_000019.9:g.51363341T>G , CM000681.1:g.51363341T>G	GRCh37
NC_000019.8:g.56055153T>G	NCBI36
NG_011653.1:g.10171T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.744T>G MANE Select	ENSP00000314151.1:p.His248Gln
ENST00000326003.6:c.744T>G	ENSP00000314151.1:p.His248Gln
ENST00000360617.7:c.1186T>G	ENSP00000353829.2:n.1186T>G
ENST00000422986.6:c.*400T>G	ENSP00000393628.2:n.*400T>G
ENST00000595392.5:c.*245T>G	ENSP00000468912.1:n.*245T>G
ENST00000595952.5:c.615T>G	ENSP00000471155.1:p.His205Gln
ENST00000596333.1:n.922T>G
ENST00000598145.1:c.746T>G
ENST00000601349.5:n.2023T>G
ENST00000601812.1:n.1176T>G
ENST00000617027.4:c.621T>G	ENSP00000483513.1:p.His207Gln
NM_001030047.1:c.*469T>G	NP_001025218.1:n.*469T>G
NM_001030048.1:c.615T>G	NP_001025219.1:p.His205Gln
NM_001648.2:c.744T>G MANE Select	NP_001639.1:p.His248Gln
XM_011526923.1:c.762T>G	XP_011525225.1:p.His254Gln
XR_935817.1:n.1324+831T>G