Canonical Allele Identifier: CA407025156

Gene: KLK3

Linked Data

• gnomAD v4: 19-50860081-T-G
• MyVariant Identifiers: chr19:g.51363337T>G (hg19) ; chr19:g.50860081T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860081T>G , CM000681.2:g.50860081T>G	GRCh38
NC_000019.9:g.51363337T>G , CM000681.1:g.51363337T>G	GRCh37
NC_000019.8:g.56055149T>G	NCBI36
NG_011653.1:g.10167T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.740T>G MANE Select	ENSP00000314151.1:p.Val247Gly
ENST00000326003.6:c.740T>G	ENSP00000314151.1:p.Val247Gly
ENST00000360617.7:c.1182T>G	ENSP00000353829.2:n.1182T>G
ENST00000422986.6:c.*396T>G	ENSP00000393628.2:n.*396T>G
ENST00000595392.5:c.*241T>G	ENSP00000468912.1:n.*241T>G
ENST00000595952.5:c.611T>G	ENSP00000471155.1:p.Val204Gly
ENST00000596333.1:n.918T>G
ENST00000598145.1:c.742T>G
ENST00000601349.5:n.2019T>G
ENST00000601812.1:n.1172T>G
ENST00000617027.4:c.617T>G	ENSP00000483513.1:p.Val206Gly
NM_001030047.1:c.*465T>G	NP_001025218.1:n.*465T>G
NM_001030048.1:c.611T>G	NP_001025219.1:p.Val204Gly
NM_001648.2:c.740T>G MANE Select	NP_001639.1:p.Val247Gly
XM_011526923.1:c.758T>G	XP_011525225.1:p.Val253Gly
XR_935817.1:n.1324+827T>G