Canonical Allele Identifier: CA9604380

Gene: KLK3

Linked Data

• dbSNP Id: rs771342720
• ExAC: 19:51361327 T / C
• gnomAD v2: 19-51361327-T-C
• gnomAD v4: 19-50858071-T-C
• MyVariant Identifiers: chr19:g.51361327T>C (hg19) ; chr19:g.50858071T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858071T>C , CM000681.2:g.50858071T>C	GRCh38
NC_000019.9:g.51361327T>C , CM000681.1:g.51361327T>C	GRCh37
NC_000019.8:g.56053139T>C	NCBI36
NG_011653.1:g.8157T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.249T>C MANE Select	ENSP00000314151.1:p.Pro83=
ENST00000326003.6:c.249T>C	ENSP00000314151.1:p.Pro83=
ENST00000360617.7:c.249T>C	ENSP00000353829.2:p.Pro83=
ENST00000422986.6:c.249T>C	ENSP00000393628.2:p.Pro83=
ENST00000593997.5:c.249T>C	ENSP00000472907.1:p.Pro83=
ENST00000595392.5:c.249T>C	ENSP00000468912.1:p.Pro83=
ENST00000595952.5:c.207-87T>C	ENSP00000471155.1:n.207-87T>C
ENST00000596185.5:c.*357T>C	ENSP00000471648.1:n.*357T>C
ENST00000596333.1:n.284T>C
ENST00000597286.5:c.138T>C	ENSP00000470523.1:p.Pro46=
ENST00000597483.5:c.207-87T>C	ENSP00000472411.1:n.207-87T>C
ENST00000598145.1:c.233T>C
ENST00000601349.5:n.1528T>C
ENST00000601503.5:c.192T>C	ENSP00000472213.1:p.Pro64=
ENST00000601812.1:n.681T>C
ENST00000617027.4:c.249T>C	ENSP00000483513.1:p.Pro83=
NM_001030047.1:c.249T>C	NP_001025218.1:p.Pro83=
NM_001030048.1:c.207-87T>C	NP_001025219.1:n.207-87T>C
NM_001648.2:c.249T>C MANE Select	NP_001639.1:p.Pro83=
XM_011526923.1:c.249T>C	XP_011525225.1:p.Pro83=
XM_011526924.1:c.249T>C	XP_011525226.1:p.Pro83=
XR_935817.1:n.284T>C