Canonical Allele Identifier: CA407025194

Gene: KLK3

Linked Data

• gnomAD v4: 19-50860099-T-A
• MyVariant Identifiers: chr19:g.51363355T>A (hg19) ; chr19:g.50860099T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860099T>A , CM000681.2:g.50860099T>A	GRCh38
NC_000019.9:g.51363355T>A , CM000681.1:g.51363355T>A	GRCh37
NC_000019.8:g.56055167T>A	NCBI36
NG_011653.1:g.10185T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.758T>A MANE Select	ENSP00000314151.1:p.Ile253Asn
ENST00000326003.6:c.758T>A	ENSP00000314151.1:p.Ile253Asn
ENST00000360617.7:c.1200T>A	ENSP00000353829.2:n.1200T>A
ENST00000422986.6:c.*414T>A	ENSP00000393628.2:n.*414T>A
ENST00000595392.5:c.*259T>A	ENSP00000468912.1:n.*259T>A
ENST00000595952.5:c.629T>A	ENSP00000471155.1:p.Ile210Asn
ENST00000596333.1:n.936T>A
ENST00000598145.1:c.760T>A
ENST00000601349.5:n.2037T>A
ENST00000601812.1:n.1190T>A
ENST00000617027.4:c.635T>A	ENSP00000483513.1:p.Ile212Asn
NM_001030047.1:c.*483T>A	NP_001025218.1:n.*483T>A
NM_001030048.1:c.629T>A	NP_001025219.1:p.Ile210Asn
NM_001648.2:c.758T>A MANE Select	NP_001639.1:p.Ile253Asn
XM_011526923.1:c.776T>A	XP_011525225.1:p.Ile259Asn
XR_935817.1:n.1324+845T>A