Canonical Allele Identifier: CA407024999

Gene: KLK3

Linked Data

• gnomAD v4: 19-50860043-T-G
• MyVariant Identifiers: chr19:g.51363299T>G (hg19) ; chr19:g.50860043T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860043T>G , CM000681.2:g.50860043T>G	GRCh38
NC_000019.9:g.51363299T>G , CM000681.1:g.51363299T>G	GRCh37
NC_000019.8:g.56055111T>G	NCBI36
NG_011653.1:g.10129T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.702T>G MANE Select	ENSP00000314151.1:p.Cys234Trp
ENST00000326003.6:c.702T>G	ENSP00000314151.1:p.Cys234Trp
ENST00000360617.7:c.1144T>G	ENSP00000353829.2:n.1144T>G
ENST00000422986.6:c.*358T>G	ENSP00000393628.2:n.*358T>G
ENST00000595392.5:c.*203T>G	ENSP00000468912.1:n.*203T>G
ENST00000595952.5:c.573T>G	ENSP00000471155.1:p.Cys191Trp
ENST00000596333.1:n.880T>G
ENST00000598145.1:c.704T>G
ENST00000601349.5:n.1981T>G
ENST00000601812.1:n.1134T>G
ENST00000617027.4:c.579T>G	ENSP00000483513.1:p.Cys193Trp
NM_001030047.1:c.*427T>G	NP_001025218.1:n.*427T>G
NM_001030048.1:c.573T>G	NP_001025219.1:p.Cys191Trp
NM_001648.2:c.702T>G MANE Select	NP_001639.1:p.Cys234Trp
XM_011526923.1:c.720T>G	XP_011525225.1:p.Cys240Trp
XR_935817.1:n.1324+789T>G