Canonical Allele Identifier: CA407025081

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363318T>G (hg19) ; chr19:g.50860062T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860062T>G , CM000681.2:g.50860062T>G	GRCh38
NC_000019.9:g.51363318T>G , CM000681.1:g.51363318T>G	GRCh37
NC_000019.8:g.56055130T>G	NCBI36
NG_011653.1:g.10148T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.721T>G MANE Select	ENSP00000314151.1:p.Ser241Ala
ENST00000326003.6:c.721T>G	ENSP00000314151.1:p.Ser241Ala
ENST00000360617.7:c.1163T>G	ENSP00000353829.2:n.1163T>G
ENST00000422986.6:c.*377T>G	ENSP00000393628.2:n.*377T>G
ENST00000595392.5:c.*222T>G	ENSP00000468912.1:n.*222T>G
ENST00000595952.5:c.592T>G	ENSP00000471155.1:p.Ser198Ala
ENST00000596333.1:n.899T>G
ENST00000598145.1:c.723T>G
ENST00000601349.5:n.2000T>G
ENST00000601812.1:n.1153T>G
ENST00000617027.4:c.598T>G	ENSP00000483513.1:p.Ser200Ala
NM_001030047.1:c.*446T>G	NP_001025218.1:n.*446T>G
NM_001030048.1:c.592T>G	NP_001025219.1:p.Ser198Ala
NM_001648.2:c.721T>G MANE Select	NP_001639.1:p.Ser241Ala
XM_011526923.1:c.739T>G	XP_011525225.1:p.Ser247Ala
XR_935817.1:n.1324+808T>G