Canonical Allele Identifier: CA508200826

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363317T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860061T>G , CM000681.2:g.50860061T>G	GRCh38
NC_000019.9:g.51363317T>G , CM000681.1:g.51363317T>G	GRCh37
NC_000019.8:g.56055129T>G	NCBI36
NG_011653.1:g.10147T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.720T>G MANE Select	ENSP00000314151.1:p.Pro240=
ENST00000326003.6:c.720T>G	ENSP00000314151.1:p.Pro240=
ENST00000360617.7:c.1162T>G	ENSP00000353829.2:n.1162T>G
ENST00000422986.6:c.*376T>G	ENSP00000393628.2:n.*376T>G
ENST00000595392.5:c.*221T>G	ENSP00000468912.1:n.*221T>G
ENST00000595952.5:c.591T>G	ENSP00000471155.1:p.Pro197=
ENST00000596333.1:n.898T>G
ENST00000598145.1:c.722T>G
ENST00000601349.5:n.1999T>G
ENST00000601812.1:n.1152T>G
ENST00000617027.4:c.597T>G	ENSP00000483513.1:p.Pro199=
NM_001030047.1:c.*445T>G	NP_001025218.1:n.*445T>G
NM_001030048.1:c.591T>G	NP_001025219.1:p.Pro197=
NM_001648.2:c.720T>G MANE Select	NP_001639.1:p.Pro240=
XM_011526923.1:c.738T>G	XP_011525225.1:p.Pro246=
XR_935817.1:n.1324+807T>G