Canonical Allele Identifier: CA508313716

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51361540C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858284C>G , CM000681.2:g.50858284C>G	GRCh38
NC_000019.9:g.51361540C>G , CM000681.1:g.51361540C>G	GRCh37
NC_000019.8:g.56053352C>G	NCBI36
NG_011653.1:g.8370C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.462C>G MANE Select	ENSP00000314151.1:p.Ala154=
ENST00000326003.6:c.462C>G	ENSP00000314151.1:p.Ala154=
ENST00000360617.7:c.462C>G	ENSP00000353829.2:p.Ala154=
ENST00000422986.6:c.*118C>G	ENSP00000393628.2:n.*118C>G
ENST00000593997.5:c.462C>G	ENSP00000472907.1:p.Ala154=
ENST00000595392.5:c.353-15C>G	ENSP00000468912.1:n.353-15C>G
ENST00000595952.5:c.333C>G	ENSP00000471155.1:p.Ala111=
ENST00000596185.5:c.*570C>G	ENSP00000471648.1:n.*570C>G
ENST00000596333.1:n.497C>G
ENST00000597286.5:c.351C>G	ENSP00000470523.1:p.Ala117=
ENST00000597483.5:c.333C>G	ENSP00000472411.1:p.Ala111=
ENST00000598145.1:c.446C>G
ENST00000601349.5:n.1741C>G
ENST00000601503.5:c.405C>G	ENSP00000472213.1:p.Ala135=
ENST00000601812.1:n.894C>G
ENST00000617027.4:c.354-15C>G	ENSP00000483513.1:n.354-15C>G
NM_001030047.1:c.462C>G	NP_001025218.1:p.Ala154=
NM_001030048.1:c.333C>G	NP_001025219.1:p.Ala111=
NM_001648.2:c.462C>G MANE Select	NP_001639.1:p.Ala154=
XM_011526923.1:c.462C>G	XP_011525225.1:p.Ala154=
XM_011526924.1:c.462C>G	XP_011525226.1:p.Ala154=
XR_935817.1:n.497C>G