Canonical Allele Identifier: CA407025039

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363310A>C (hg19) ; chr19:g.50860054A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860054A>C , CM000681.2:g.50860054A>C	GRCh38
NC_000019.9:g.51363310A>C , CM000681.1:g.51363310A>C	GRCh37
NC_000019.8:g.56055122A>C	NCBI36
NG_011653.1:g.10140A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.713A>C MANE Select	ENSP00000314151.1:p.Glu238Ala
ENST00000326003.6:c.713A>C	ENSP00000314151.1:p.Glu238Ala
ENST00000360617.7:c.1155A>C	ENSP00000353829.2:n.1155A>C
ENST00000422986.6:c.*369A>C	ENSP00000393628.2:n.*369A>C
ENST00000595392.5:c.*214A>C	ENSP00000468912.1:n.*214A>C
ENST00000595952.5:c.584A>C	ENSP00000471155.1:p.Glu195Ala
ENST00000596333.1:n.891A>C
ENST00000598145.1:c.715A>C
ENST00000601349.5:n.1992A>C
ENST00000601812.1:n.1145A>C
ENST00000617027.4:c.590A>C	ENSP00000483513.1:p.Glu197Ala
NM_001030047.1:c.*438A>C	NP_001025218.1:n.*438A>C
NM_001030048.1:c.584A>C	NP_001025219.1:p.Glu195Ala
NM_001648.2:c.713A>C MANE Select	NP_001639.1:p.Glu238Ala
XM_011526923.1:c.731A>C	XP_011525225.1:p.Glu244Ala
XR_935817.1:n.1324+800A>C