Canonical Allele Identifier: CA633899595

Gene: KLK3

Linked Data

• dbSNP Id: rs1460551339
• gnomAD v2: 19-51363390-CT-C
• gnomAD v4: 19-50860134-CT-C
• MyVariant Identifiers: chr19:g.51363391del (hg19) ; chr19:g.50860135del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860135del , CM000681.2:g.50860135del	GRCh38
NC_000019.9:g.51363391del , CM000681.1:g.51363391del	GRCh37
NC_000019.8:g.56055203del	NCBI36
NG_011653.1:g.10221del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.*8del MANE Select	ENSP00000314151.1:n.*8del
ENST00000326003.6:c.*8del	ENSP00000314151.1:n.*8del
ENST00000360617.7:c.1236del	ENSP00000353829.2:n.1236del
ENST00000422986.6:c.*450del	ENSP00000393628.2:n.*450del
ENST00000595392.5:c.*295del	ENSP00000468912.1:n.*295del
ENST00000595952.5:c.*8del	ENSP00000471155.1:n.*8del
ENST00000596333.1:n.972del
ENST00000598145.1:c.796del
ENST00000601349.5:n.2073del
ENST00000617027.4:c.*8del	ENSP00000483513.1:n.*8del
NM_001030047.1:c.*519del	NP_001025218.1:n.*519del
NM_001030048.1:c.*8del	NP_001025219.1:n.*8del
NM_001648.2:c.*8del MANE Select	NP_001639.1:n.*8del
XM_011526923.1:c.*8del	XP_011525225.1:n.*8del
XR_935817.1:n.1324+881del