Canonical Allele Identifier: CA508200860

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363374C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860118C>G , CM000681.2:g.50860118C>G	GRCh38
NC_000019.9:g.51363374C>G , CM000681.1:g.51363374C>G	GRCh37
NC_000019.8:g.56055186C>G	NCBI36
NG_011653.1:g.10204C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.777C>G MANE Select	ENSP00000314151.1:p.Ala259=
ENST00000326003.6:c.777C>G	ENSP00000314151.1:p.Ala259=
ENST00000360617.7:c.1219C>G	ENSP00000353829.2:n.1219C>G
ENST00000422986.6:c.*433C>G	ENSP00000393628.2:n.*433C>G
ENST00000595392.5:c.*278C>G	ENSP00000468912.1:n.*278C>G
ENST00000595952.5:c.648C>G	ENSP00000471155.1:p.Ala216=
ENST00000596333.1:n.955C>G
ENST00000598145.1:c.779C>G
ENST00000601349.5:n.2056C>G
ENST00000601812.1:n.1209C>G
ENST00000617027.4:c.654C>G	ENSP00000483513.1:p.Ala218=
NM_001030047.1:c.*502C>G	NP_001025218.1:n.*502C>G
NM_001030048.1:c.648C>G	NP_001025219.1:p.Ala216=
NM_001648.2:c.777C>G MANE Select	NP_001639.1:p.Ala259=
XM_011526923.1:c.795C>G	XP_011525225.1:p.Ala265=
XR_935817.1:n.1324+864C>G