Canonical Allele Identifier: CA407022586

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51361466G>T (hg19) ; chr19:g.50858210G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858210G>T , CM000681.2:g.50858210G>T	GRCh38
NC_000019.9:g.51361466G>T , CM000681.1:g.51361466G>T	GRCh37
NC_000019.8:g.56053278G>T	NCBI36
NG_011653.1:g.8296G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.388G>T MANE Select	ENSP00000314151.1:p.Ala130Ser
ENST00000326003.6:c.388G>T	ENSP00000314151.1:p.Ala130Ser
ENST00000360617.7:c.388G>T	ENSP00000353829.2:p.Ala130Ser
ENST00000422986.6:c.*44G>T	ENSP00000393628.2:n.*44G>T
ENST00000593997.5:c.388G>T	ENSP00000472907.1:p.Ala130Ser
ENST00000595392.5:c.352+36G>T	ENSP00000468912.1:n.352+36G>T
ENST00000595952.5:c.259G>T	ENSP00000471155.1:p.Ala87Ser
ENST00000596185.5:c.*496G>T	ENSP00000471648.1:n.*496G>T
ENST00000596333.1:n.423G>T
ENST00000597286.5:c.277G>T	ENSP00000470523.1:p.Ala93Ser
ENST00000597483.5:c.259G>T	ENSP00000472411.1:p.Ala87Ser
ENST00000598145.1:c.372G>T
ENST00000601349.5:n.1667G>T
ENST00000601503.5:c.331G>T	ENSP00000472213.1:p.Ala111Ser
ENST00000601812.1:n.820G>T
ENST00000617027.4:c.353+35G>T	ENSP00000483513.1:n.353+35G>T
NM_001030047.1:c.388G>T	NP_001025218.1:p.Ala130Ser
NM_001030048.1:c.259G>T	NP_001025219.1:p.Ala87Ser
NM_001648.2:c.388G>T MANE Select	NP_001639.1:p.Ala130Ser
XM_011526923.1:c.388G>T	XP_011525225.1:p.Ala130Ser
XM_011526924.1:c.388G>T	XP_011525226.1:p.Ala130Ser
XR_935817.1:n.423G>T