Canonical Allele Identifier: CA2586638926

Gene: KLK3

Linked Data

• gnomAD v4: 19-50860193-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860193G>T , CM000681.2:g.50860193G>T	GRCh38
NC_000019.9:g.51363449G>T , CM000681.1:g.51363449G>T	GRCh37
NC_000019.8:g.56055261G>T	NCBI36
NG_011653.1:g.10279G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.*66G>T MANE Select	ENSP00000314151.1:n.*66G>T
ENST00000326003.6:c.*66G>T	ENSP00000314151.1:n.*66G>T
ENST00000360617.7:c.1294G>T	ENSP00000353829.2:n.1294G>T
ENST00000422986.6:c.*508G>T	ENSP00000393628.2:n.*508G>T
ENST00000595392.5:c.*353G>T	ENSP00000468912.1:n.*353G>T
ENST00000595952.5:c.*66G>T	ENSP00000471155.1:n.*66G>T
ENST00000596333.1:n.1030G>T
ENST00000598145.1:c.854G>T
ENST00000601349.5:n.2131G>T
ENST00000617027.4:c.*66G>T	ENSP00000483513.1:n.*66G>T
NM_001030047.1:c.*577G>T	NP_001025218.1:n.*577G>T
NM_001030048.1:c.*66G>T	NP_001025219.1:n.*66G>T
NM_001648.2:c.*66G>T MANE Select	NP_001639.1:n.*66G>T
XM_011526923.1:c.*66G>T	XP_011525225.1:n.*66G>T
XR_935817.1:n.1324+939G>T