Canonical Allele Identifier: CA407022744

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51361517G>C (hg19) ; chr19:g.50858261G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858261G>C , CM000681.2:g.50858261G>C	GRCh38
NC_000019.9:g.51361517G>C , CM000681.1:g.51361517G>C	GRCh37
NC_000019.8:g.56053329G>C	NCBI36
NG_011653.1:g.8347G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.439G>C MANE Select	ENSP00000314151.1:p.Ala147Pro
ENST00000326003.6:c.439G>C	ENSP00000314151.1:p.Ala147Pro
ENST00000360617.7:c.439G>C	ENSP00000353829.2:p.Ala147Pro
ENST00000422986.6:c.*95G>C	ENSP00000393628.2:n.*95G>C
ENST00000593997.5:c.439G>C	ENSP00000472907.1:p.Ala147Pro
ENST00000595392.5:c.353-38G>C	ENSP00000468912.1:n.353-38G>C
ENST00000595952.5:c.310G>C	ENSP00000471155.1:p.Ala104Pro
ENST00000596185.5:c.*547G>C	ENSP00000471648.1:n.*547G>C
ENST00000596333.1:n.474G>C
ENST00000597286.5:c.328G>C	ENSP00000470523.1:p.Ala110Pro
ENST00000597483.5:c.310G>C	ENSP00000472411.1:p.Ala104Pro
ENST00000598145.1:c.423G>C
ENST00000601349.5:n.1718G>C
ENST00000601503.5:c.382G>C	ENSP00000472213.1:p.Ala128Pro
ENST00000601812.1:n.871G>C
ENST00000617027.4:c.354-38G>C	ENSP00000483513.1:n.354-38G>C
NM_001030047.1:c.439G>C	NP_001025218.1:p.Ala147Pro
NM_001030048.1:c.310G>C	NP_001025219.1:p.Ala104Pro
NM_001648.2:c.439G>C MANE Select	NP_001639.1:p.Ala147Pro
XM_011526923.1:c.439G>C	XP_011525225.1:p.Ala147Pro
XM_011526924.1:c.439G>C	XP_011525226.1:p.Ala147Pro
XR_935817.1:n.474G>C