Canonical Allele Identifier: CA2586636959

Gene: KLK3

Linked Data

• gnomAD v4: 19-50856847-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50856847G>T , CM000681.2:g.50856847G>T	GRCh38
NC_000019.9:g.51360103G>T , CM000681.1:g.51360103G>T	GRCh37
NC_000019.8:g.56051915G>T	NCBI36
NG_011653.1:g.6933G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.206+448G>T MANE Select	ENSP00000314151.1:n.206+448G>T
ENST00000326003.6:c.206+448G>T	ENSP00000314151.1:n.206+448G>T
ENST00000360617.7:c.206+448G>T	ENSP00000353829.2:n.206+448G>T
ENST00000422986.6:c.206+448G>T	ENSP00000393628.2:n.206+448G>T
ENST00000593997.5:c.206+448G>T	ENSP00000472907.1:n.206+448G>T
ENST00000595392.5:c.206+448G>T	ENSP00000468912.1:n.206+448G>T
ENST00000595952.5:c.206+448G>T	ENSP00000471155.1:n.206+448G>T
ENST00000596185.5:c.*314+448G>T	ENSP00000471648.1:n.*314+448G>T
ENST00000596333.1:n.241+448G>T
ENST00000597286.5:c.95+448G>T	ENSP00000470523.1:n.95+448G>T
ENST00000597483.5:c.206+448G>T	ENSP00000472411.1:n.206+448G>T
ENST00000598145.1:c.190+448G>T
ENST00000601349.5:n.1485+448G>T
ENST00000601503.5:c.149+448G>T	ENSP00000472213.1:n.149+448G>T
ENST00000617027.4:c.206+448G>T	ENSP00000483513.1:n.206+448G>T
NM_001030047.1:c.206+448G>T	NP_001025218.1:n.206+448G>T
NM_001030048.1:c.206+448G>T	NP_001025219.1:n.206+448G>T
NM_001648.2:c.206+448G>T MANE Select	NP_001639.1:n.206+448G>T
XM_011526923.1:c.206+448G>T	XP_011525225.1:n.206+448G>T
XM_011526924.1:c.206+448G>T	XP_011525226.1:n.206+448G>T
XR_935817.1:n.241+448G>T