Canonical Allele Identifier: CA633705880

Gene: KLK3

Linked Data

• dbSNP Id: rs1419767084
• gnomAD v2: 19-51363595-C-T
• gnomAD v3: 19-50860339-C-T
• gnomAD v4: 19-50860339-C-T
• MyVariant Identifiers: chr19:g.51363595C>T (hg19) ; chr19:g.50860339C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860339C>T , CM000681.2:g.50860339C>T	GRCh38
NC_000019.9:g.51363595C>T , CM000681.1:g.51363595C>T	GRCh37
NC_000019.8:g.56055407C>T	NCBI36
NG_011653.1:g.10425C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.*212C>T MANE Select	ENSP00000314151.1:n.*212C>T
ENST00000326003.6:c.*212C>T	ENSP00000314151.1:n.*212C>T
ENST00000360617.7:c.1440C>T	ENSP00000353829.2:n.1440C>T
ENST00000422986.6:c.*654C>T	ENSP00000393628.2:n.*654C>T
ENST00000595952.5:c.*212C>T	ENSP00000471155.1:n.*212C>T
ENST00000596333.1:n.1176C>T
ENST00000601349.5:n.2277C>T
ENST00000617027.4:c.*212C>T	ENSP00000483513.1:n.*212C>T
NM_001030047.1:c.*723C>T	NP_001025218.1:n.*723C>T
NM_001030048.1:c.*212C>T	NP_001025219.1:n.*212C>T
NM_001648.2:c.*212C>T MANE Select	NP_001639.1:n.*212C>T
XM_011526923.1:c.*212C>T	XP_011525225.1:n.*212C>T
XR_935817.1:n.1324+1085C>T