Canonical Allele Identifier: CA508200821

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363308C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860052C>A , CM000681.2:g.50860052C>A	GRCh38
NC_000019.9:g.51363308C>A , CM000681.1:g.51363308C>A	GRCh37
NC_000019.8:g.56055120C>A	NCBI36
NG_011653.1:g.10138C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.711C>A MANE Select	ENSP00000314151.1:p.Pro237=
ENST00000326003.6:c.711C>A	ENSP00000314151.1:p.Pro237=
ENST00000360617.7:c.1153C>A	ENSP00000353829.2:n.1153C>A
ENST00000422986.6:c.*367C>A	ENSP00000393628.2:n.*367C>A
ENST00000595392.5:c.*212C>A	ENSP00000468912.1:n.*212C>A
ENST00000595952.5:c.582C>A	ENSP00000471155.1:p.Pro194=
ENST00000596333.1:n.889C>A
ENST00000598145.1:c.713C>A
ENST00000601349.5:n.1990C>A
ENST00000601812.1:n.1143C>A
ENST00000617027.4:c.588C>A	ENSP00000483513.1:p.Pro196=
NM_001030047.1:c.*436C>A	NP_001025218.1:n.*436C>A
NM_001030048.1:c.582C>A	NP_001025219.1:p.Pro194=
NM_001648.2:c.711C>A MANE Select	NP_001639.1:p.Pro237=
XM_011526923.1:c.729C>A	XP_011525225.1:p.Pro243=
XR_935817.1:n.1324+798C>A