Canonical Allele Identifier: CA309634004

Gene: KLK3

Linked Data

• dbSNP Id: rs548476435
• gnomAD v4: 19-50860098-A-G
• MyVariant Identifiers: chr19:g.51363354A>G (hg19) ; chr19:g.50860098A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860098A>G , CM000681.2:g.50860098A>G	GRCh38
NC_000019.9:g.51363354A>G , CM000681.1:g.51363354A>G	GRCh37
NC_000019.8:g.56055166A>G	NCBI36
NG_011653.1:g.10184A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.757A>G MANE Select	ENSP00000314151.1:p.Ile253Val
ENST00000326003.6:c.757A>G	ENSP00000314151.1:p.Ile253Val
ENST00000360617.7:c.1199A>G	ENSP00000353829.2:n.1199A>G
ENST00000422986.6:c.*413A>G	ENSP00000393628.2:n.*413A>G
ENST00000595392.5:c.*258A>G	ENSP00000468912.1:n.*258A>G
ENST00000595952.5:c.628A>G	ENSP00000471155.1:p.Ile210Val
ENST00000596333.1:n.935A>G
ENST00000598145.1:c.759A>G
ENST00000601349.5:n.2036A>G
ENST00000601812.1:n.1189A>G
ENST00000617027.4:c.634A>G	ENSP00000483513.1:p.Ile212Val
NM_001030047.1:c.*482A>G	NP_001025218.1:n.*482A>G
NM_001030048.1:c.628A>G	NP_001025219.1:p.Ile210Val
NM_001648.2:c.757A>G MANE Select	NP_001639.1:p.Ile253Val
XM_011526923.1:c.775A>G	XP_011525225.1:p.Ile259Val
XR_935817.1:n.1324+844A>G