Canonical Allele Identifier: CA508200796

Gene: KLK3

Linked Data

• dbSNP Id: rs1294929483
• gnomAD v2: 19-51363269-A-G
• gnomAD v3: 19-50860013-A-G
• gnomAD v4: 19-50860013-A-G
• MyVariant Identifiers: chr19:g.51363269A>G (hg19) ; chr19:g.50860013A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860013A>G , CM000681.2:g.50860013A>G	GRCh38
NC_000019.9:g.51363269A>G , CM000681.1:g.51363269A>G	GRCh37
NC_000019.8:g.56055081A>G	NCBI36
NG_011653.1:g.10099A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.672A>G MANE Select	ENSP00000314151.1:p.Gln224=
ENST00000326003.6:c.672A>G	ENSP00000314151.1:p.Gln224=
ENST00000360617.7:c.1114A>G	ENSP00000353829.2:n.1114A>G
ENST00000422986.6:c.*328A>G	ENSP00000393628.2:n.*328A>G
ENST00000595392.5:c.*173A>G	ENSP00000468912.1:n.*173A>G
ENST00000595952.5:c.543A>G	ENSP00000471155.1:p.Gln181=
ENST00000596333.1:n.850A>G
ENST00000598145.1:c.674A>G
ENST00000601349.5:n.1951A>G
ENST00000601812.1:n.1104A>G
ENST00000617027.4:c.549A>G	ENSP00000483513.1:p.Gln183=
NM_001030047.1:c.*397A>G	NP_001025218.1:n.*397A>G
NM_001030048.1:c.543A>G	NP_001025219.1:p.Gln181=
NM_001648.2:c.672A>G MANE Select	NP_001639.1:p.Gln224=
XM_011526923.1:c.690A>G	XP_011525225.1:p.Gln230=
XR_935817.1:n.1324+759A>G