Canonical Allele Identifier: CA508200858

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363371G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860115G>T , CM000681.2:g.50860115G>T	GRCh38
NC_000019.9:g.51363371G>T , CM000681.1:g.51363371G>T	GRCh37
NC_000019.8:g.56055183G>T	NCBI36
NG_011653.1:g.10201G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.774G>T MANE Select	ENSP00000314151.1:p.Val258=
ENST00000326003.6:c.774G>T	ENSP00000314151.1:p.Val258=
ENST00000360617.7:c.1216G>T	ENSP00000353829.2:n.1216G>T
ENST00000422986.6:c.*430G>T	ENSP00000393628.2:n.*430G>T
ENST00000595392.5:c.*275G>T	ENSP00000468912.1:n.*275G>T
ENST00000595952.5:c.645G>T	ENSP00000471155.1:p.Val215=
ENST00000596333.1:n.952G>T
ENST00000598145.1:c.776G>T
ENST00000601349.5:n.2053G>T
ENST00000601812.1:n.1206G>T
ENST00000617027.4:c.651G>T	ENSP00000483513.1:p.Val217=
NM_001030047.1:c.*499G>T	NP_001025218.1:n.*499G>T
NM_001030048.1:c.645G>T	NP_001025219.1:p.Val215=
NM_001648.2:c.774G>T MANE Select	NP_001639.1:p.Val258=
XM_011526923.1:c.792G>T	XP_011525225.1:p.Val264=
XR_935817.1:n.1324+861G>T