Canonical Allele Identifier: CA508313357

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51361546C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858290C>G , CM000681.2:g.50858290C>G	GRCh38
NC_000019.9:g.51361546C>G , CM000681.1:g.51361546C>G	GRCh37
NC_000019.8:g.56053358C>G	NCBI36
NG_011653.1:g.8376C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.468C>G MANE Select	ENSP00000314151.1:p.Gly156=
ENST00000326003.6:c.468C>G	ENSP00000314151.1:p.Gly156=
ENST00000360617.7:c.468C>G	ENSP00000353829.2:p.Gly156=
ENST00000422986.6:c.*124C>G	ENSP00000393628.2:n.*124C>G
ENST00000593997.5:c.468C>G	ENSP00000472907.1:p.Gly156=
ENST00000595392.5:c.353-9C>G	ENSP00000468912.1:n.353-9C>G
ENST00000595952.5:c.339C>G	ENSP00000471155.1:p.Gly113=
ENST00000596185.5:c.*576C>G	ENSP00000471648.1:n.*576C>G
ENST00000596333.1:n.503C>G
ENST00000597286.5:c.357C>G	ENSP00000470523.1:p.Gly119=
ENST00000597483.5:c.339C>G	ENSP00000472411.1:p.Gly113=
ENST00000598145.1:c.452C>G
ENST00000601349.5:n.1747C>G
ENST00000601503.5:c.411C>G	ENSP00000472213.1:p.Gly137=
ENST00000601812.1:n.900C>G
ENST00000617027.4:c.354-9C>G	ENSP00000483513.1:n.354-9C>G
NM_001030047.1:c.468C>G	NP_001025218.1:p.Gly156=
NM_001030048.1:c.339C>G	NP_001025219.1:p.Gly113=
NM_001648.2:c.468C>G MANE Select	NP_001639.1:p.Gly156=
XM_011526923.1:c.468C>G	XP_011525225.1:p.Gly156=
XM_011526924.1:c.468C>G	XP_011525226.1:p.Gly156=
XR_935817.1:n.503C>G