Canonical Allele Identifier: CA508200828

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363320C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860064C>T , CM000681.2:g.50860064C>T	GRCh38
NC_000019.9:g.51363320C>T , CM000681.1:g.51363320C>T	GRCh37
NC_000019.8:g.56055132C>T	NCBI36
NG_011653.1:g.10150C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.723C>T MANE Select	ENSP00000314151.1:p.Ser241=
ENST00000326003.6:c.723C>T	ENSP00000314151.1:p.Ser241=
ENST00000360617.7:c.1165C>T	ENSP00000353829.2:n.1165C>T
ENST00000422986.6:c.*379C>T	ENSP00000393628.2:n.*379C>T
ENST00000595392.5:c.*224C>T	ENSP00000468912.1:n.*224C>T
ENST00000595952.5:c.594C>T	ENSP00000471155.1:p.Ser198=
ENST00000596333.1:n.901C>T
ENST00000598145.1:c.725C>T
ENST00000601349.5:n.2002C>T
ENST00000601812.1:n.1155C>T
ENST00000617027.4:c.600C>T	ENSP00000483513.1:p.Ser200=
NM_001030047.1:c.*448C>T	NP_001025218.1:n.*448C>T
NM_001030048.1:c.594C>T	NP_001025219.1:p.Ser198=
NM_001648.2:c.723C>T MANE Select	NP_001639.1:p.Ser241=
XM_011526923.1:c.741C>T	XP_011525225.1:p.Ser247=
XR_935817.1:n.1324+810C>T