Canonical Allele Identifier: CA309634035

Gene: KLK3

Linked Data

• dbSNP Id: rs927948898
• gnomAD v2: 19-51363367-T-A
• gnomAD v3: 19-50860111-T-A
• gnomAD v4: 19-50860111-T-A
• MyVariant Identifiers: chr19:g.51363367T>A (hg19) ; chr19:g.50860111T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860111T>A , CM000681.2:g.50860111T>A	GRCh38
NC_000019.9:g.51363367T>A , CM000681.1:g.51363367T>A	GRCh37
NC_000019.8:g.56055179T>A	NCBI36
NG_011653.1:g.10197T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.770T>A MANE Select	ENSP00000314151.1:p.Ile257Asn
ENST00000326003.6:c.770T>A	ENSP00000314151.1:p.Ile257Asn
ENST00000360617.7:c.1212T>A	ENSP00000353829.2:n.1212T>A
ENST00000422986.6:c.*426T>A	ENSP00000393628.2:n.*426T>A
ENST00000595392.5:c.*271T>A	ENSP00000468912.1:n.*271T>A
ENST00000595952.5:c.641T>A	ENSP00000471155.1:p.Ile214Asn
ENST00000596333.1:n.948T>A
ENST00000598145.1:c.772T>A
ENST00000601349.5:n.2049T>A
ENST00000601812.1:n.1202T>A
ENST00000617027.4:c.647T>A	ENSP00000483513.1:p.Ile216Asn
NM_001030047.1:c.*495T>A	NP_001025218.1:n.*495T>A
NM_001030048.1:c.641T>A	NP_001025219.1:p.Ile214Asn
NM_001648.2:c.770T>A MANE Select	NP_001639.1:p.Ile257Asn
XM_011526923.1:c.788T>A	XP_011525225.1:p.Ile263Asn
XR_935817.1:n.1324+857T>A