Canonical Allele Identifier: CA9604625

Gene: KLK3

Linked Data

• dbSNP Id: rs374859717
• ExAC: 19:51363413 A / G
• gnomAD v2: 19-51363413-A-G
• MyVariant Identifiers: chr19:g.51363413A>G (hg19) ; chr19:g.50860157A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860157A>G , CM000681.2:g.50860157A>G	GRCh38
NC_000019.9:g.51363413A>G , CM000681.1:g.51363413A>G	GRCh37
NC_000019.8:g.56055225A>G	NCBI36
NG_011653.1:g.10243A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.*30A>G MANE Select	ENSP00000314151.1:n.*30A>G
ENST00000326003.6:c.*30A>G	ENSP00000314151.1:n.*30A>G
ENST00000360617.7:c.1258A>G	ENSP00000353829.2:n.1258A>G
ENST00000422986.6:c.*472A>G	ENSP00000393628.2:n.*472A>G
ENST00000595392.5:c.*317A>G	ENSP00000468912.1:n.*317A>G
ENST00000595952.5:c.*30A>G	ENSP00000471155.1:n.*30A>G
ENST00000596333.1:n.994A>G
ENST00000598145.1:c.818A>G
ENST00000601349.5:n.2095A>G
ENST00000617027.4:c.*30A>G	ENSP00000483513.1:n.*30A>G
NM_001030047.1:c.*541A>G	NP_001025218.1:n.*541A>G
NM_001030048.1:c.*30A>G	NP_001025219.1:n.*30A>G
NM_001648.2:c.*30A>G MANE Select	NP_001639.1:n.*30A>G
XM_011526923.1:c.*30A>G	XP_011525225.1:n.*30A>G
XR_935817.1:n.1324+903A>G