Canonical Allele Identifier: CA407025196

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363357A>C (hg19) ; chr19:g.50860101A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860101A>C , CM000681.2:g.50860101A>C	GRCh38
NC_000019.9:g.51363357A>C , CM000681.1:g.51363357A>C	GRCh37
NC_000019.8:g.56055169A>C	NCBI36
NG_011653.1:g.10187A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.760A>C MANE Select	ENSP00000314151.1:p.Lys254Gln
ENST00000326003.6:c.760A>C	ENSP00000314151.1:p.Lys254Gln
ENST00000360617.7:c.1202A>C	ENSP00000353829.2:n.1202A>C
ENST00000422986.6:c.*416A>C	ENSP00000393628.2:n.*416A>C
ENST00000595392.5:c.*261A>C	ENSP00000468912.1:n.*261A>C
ENST00000595952.5:c.631A>C	ENSP00000471155.1:p.Lys211Gln
ENST00000596333.1:n.938A>C
ENST00000598145.1:c.762A>C
ENST00000601349.5:n.2039A>C
ENST00000601812.1:n.1192A>C
ENST00000617027.4:c.637A>C	ENSP00000483513.1:p.Lys213Gln
NM_001030047.1:c.*485A>C	NP_001025218.1:n.*485A>C
NM_001030048.1:c.631A>C	NP_001025219.1:p.Lys211Gln
NM_001648.2:c.760A>C MANE Select	NP_001639.1:p.Lys254Gln
XM_011526923.1:c.778A>C	XP_011525225.1:p.Lys260Gln
XR_935817.1:n.1324+847A>C