Canonical Allele Identifier: CA508313369

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51361564A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858308A>G , CM000681.2:g.50858308A>G	GRCh38
NC_000019.9:g.51361564A>G , CM000681.1:g.51361564A>G	GRCh37
NC_000019.8:g.56053376A>G	NCBI36
NG_011653.1:g.8394A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.486A>G MANE Select	ENSP00000314151.1:p.Pro162=
ENST00000326003.6:c.486A>G	ENSP00000314151.1:p.Pro162=
ENST00000360617.7:c.486A>G	ENSP00000353829.2:p.Pro162=
ENST00000422986.6:c.*142A>G	ENSP00000393628.2:n.*142A>G
ENST00000593997.5:c.486A>G	ENSP00000472907.1:p.Pro162=
ENST00000595392.5:c.362A>G	ENSP00000468912.1:p.Gln121Arg
ENST00000595952.5:c.357A>G	ENSP00000471155.1:p.Pro119=
ENST00000596185.5:c.*594A>G	ENSP00000471648.1:n.*594A>G
ENST00000596333.1:n.521A>G
ENST00000597286.5:c.375A>G	ENSP00000470523.1:p.Pro125=
ENST00000597483.5:c.357A>G	ENSP00000472411.1:p.Pro119=
ENST00000598145.1:c.470A>G
ENST00000601349.5:n.1765A>G
ENST00000601503.5:c.429A>G	ENSP00000472213.1:p.Pro143=
ENST00000601812.1:n.918A>G
ENST00000617027.4:c.363A>G	ENSP00000483513.1:p.Pro121=
NM_001030047.1:c.486A>G	NP_001025218.1:p.Pro162=
NM_001030048.1:c.357A>G	NP_001025219.1:p.Pro119=
NM_001648.2:c.486A>G MANE Select	NP_001639.1:p.Pro162=
XM_011526923.1:c.486A>G	XP_011525225.1:p.Pro162=
XM_011526924.1:c.486A>G	XP_011525226.1:p.Pro162=
XR_935817.1:n.521A>G