Canonical Allele Identifier: CA407024825

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363232A>C (hg19) ; chr19:g.50859976A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50859976A>C , CM000681.2:g.50859976A>C	GRCh38
NC_000019.9:g.51363232A>C , CM000681.1:g.51363232A>C	GRCh37
NC_000019.8:g.56055044A>C	NCBI36
NG_011653.1:g.10062A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.635A>C MANE Select	ENSP00000314151.1:p.Asp212Ala
ENST00000326003.6:c.635A>C	ENSP00000314151.1:p.Asp212Ala
ENST00000360617.7:c.1077A>C	ENSP00000353829.2:n.1077A>C
ENST00000422986.6:c.*291A>C	ENSP00000393628.2:n.*291A>C
ENST00000595392.5:c.*136A>C	ENSP00000468912.1:n.*136A>C
ENST00000595952.5:c.506A>C	ENSP00000471155.1:p.Asp169Ala
ENST00000596185.5:c.*743A>C	ENSP00000471648.1:n.*743A>C
ENST00000596333.1:n.813A>C
ENST00000598145.1:c.637A>C
ENST00000601349.5:n.1914A>C
ENST00000601812.1:n.1067A>C
ENST00000617027.4:c.512A>C	ENSP00000483513.1:p.Asp171Ala
NM_001030047.1:c.*360A>C	NP_001025218.1:n.*360A>C
NM_001030048.1:c.506A>C	NP_001025219.1:p.Asp169Ala
NM_001648.2:c.635A>C MANE Select	NP_001639.1:p.Asp212Ala
XM_011526923.1:c.653A>C	XP_011525225.1:p.Asp218Ala
XM_011526924.1:c.*360A>C	XP_011525226.1:n.*360A>C
XR_935817.1:n.1324+722A>C