Canonical Allele Identifier: CA2586638824

Gene: KLK3

Linked Data

• gnomAD v4: 19-50859757-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50859757G>T , CM000681.2:g.50859757G>T	GRCh38
NC_000019.9:g.51363013G>T , CM000681.1:g.51363013G>T	GRCh37
NC_000019.8:g.56054825G>T	NCBI36
NG_011653.1:g.9843G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.631-215G>T MANE Select	ENSP00000314151.1:n.631-215G>T
ENST00000326003.6:c.631-215G>T	ENSP00000314151.1:n.631-215G>T
ENST00000360617.7:c.858G>T	ENSP00000353829.2:n.858G>T
ENST00000422986.6:c.*287-215G>T	ENSP00000393628.2:n.*287-215G>T
ENST00000595392.5:c.*132-215G>T	ENSP00000468912.1:n.*132-215G>T
ENST00000595952.5:c.502-215G>T	ENSP00000471155.1:n.502-215G>T
ENST00000596185.5:c.*739-215G>T	ENSP00000471648.1:n.*739-215G>T
ENST00000596333.1:n.809-215G>T
ENST00000597483.5:c.*141G>T	ENSP00000472411.1:n.*141G>T
ENST00000598145.1:c.633-215G>T
ENST00000601349.5:n.1910-215G>T
ENST00000601812.1:n.1063-215G>T
ENST00000617027.4:c.508-215G>T	ENSP00000483513.1:n.508-215G>T
NM_001030047.1:c.*141G>T	NP_001025218.1:n.*141G>T
NM_001030048.1:c.502-215G>T	NP_001025219.1:n.502-215G>T
NM_001648.2:c.631-215G>T MANE Select	NP_001639.1:n.631-215G>T
XM_011526923.1:c.649-215G>T	XP_011525225.1:n.649-215G>T
XM_011526924.1:c.*141G>T	XP_011525226.1:n.*141G>T
XR_935817.1:n.1324+503G>T