Canonical Allele Identifier: CA407025071

Gene: KLK3

Linked Data

• gnomAD v4: 19-50860060-C-A
• MyVariant Identifiers: chr19:g.51363316C>A (hg19) ; chr19:g.50860060C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860060C>A , CM000681.2:g.50860060C>A	GRCh38
NC_000019.9:g.51363316C>A , CM000681.1:g.51363316C>A	GRCh37
NC_000019.8:g.56055128C>A	NCBI36
NG_011653.1:g.10146C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.719C>A MANE Select	ENSP00000314151.1:p.Pro240His
ENST00000326003.6:c.719C>A	ENSP00000314151.1:p.Pro240His
ENST00000360617.7:c.1161C>A	ENSP00000353829.2:n.1161C>A
ENST00000422986.6:c.*375C>A	ENSP00000393628.2:n.*375C>A
ENST00000595392.5:c.*220C>A	ENSP00000468912.1:n.*220C>A
ENST00000595952.5:c.590C>A	ENSP00000471155.1:p.Pro197His
ENST00000596333.1:n.897C>A
ENST00000598145.1:c.721C>A
ENST00000601349.5:n.1998C>A
ENST00000601812.1:n.1151C>A
ENST00000617027.4:c.596C>A	ENSP00000483513.1:p.Pro199His
NM_001030047.1:c.*444C>A	NP_001025218.1:n.*444C>A
NM_001030048.1:c.590C>A	NP_001025219.1:p.Pro197His
NM_001648.2:c.719C>A MANE Select	NP_001639.1:p.Pro240His
XM_011526923.1:c.737C>A	XP_011525225.1:p.Pro246His
XR_935817.1:n.1324+806C>A