Canonical Allele Identifier: CA508200848
Gene: KLK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.51363350G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50860094G>A , CM000681.2:g.50860094G>A GRCh38
NC_000019.9:g.51363350G>A , CM000681.1:g.51363350G>A GRCh37
NC_000019.8:g.56055162G>A NCBI36
NG_011653.1:g.10180G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.753G>A MANE Select ENSP00000314151.1:p.Lys251=
ENST00000326003.6:c.753G>A ENSP00000314151.1:p.Lys251=
ENST00000360617.7:c.1195G>A ENSP00000353829.2:n.1195G>A
ENST00000422986.6:c.*409G>A ENSP00000393628.2:n.*409G>A
ENST00000595392.5:c.*254G>A ENSP00000468912.1:n.*254G>A
ENST00000595952.5:c.624G>A ENSP00000471155.1:p.Lys208=
ENST00000596333.1:n.931G>A
ENST00000598145.1:c.755G>A
ENST00000601349.5:n.2032G>A
ENST00000601812.1:n.1185G>A
ENST00000617027.4:c.630G>A ENSP00000483513.1:p.Lys210=
NM_001030047.1:c.*478G>A NP_001025218.1:n.*478G>A
NM_001030048.1:c.624G>A NP_001025219.1:p.Lys208=
NM_001648.2:c.753G>A MANE Select NP_001639.1:p.Lys251=
XM_011526923.1:c.771G>A XP_011525225.1:p.Lys257=
XR_935817.1:n.1324+840G>A