Canonical Allele Identifier: CA2586639278

Gene: KLK3

Linked Data

• gnomAD v4: 19-50860174-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860174T>C , CM000681.2:g.50860174T>C	GRCh38
NC_000019.9:g.51363430T>C , CM000681.1:g.51363430T>C	GRCh37
NC_000019.8:g.56055242T>C	NCBI36
NG_011653.1:g.10260T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.*47T>C MANE Select	ENSP00000314151.1:n.*47T>C
ENST00000326003.6:c.*47T>C	ENSP00000314151.1:n.*47T>C
ENST00000360617.7:c.1275T>C	ENSP00000353829.2:n.1275T>C
ENST00000422986.6:c.*489T>C	ENSP00000393628.2:n.*489T>C
ENST00000595392.5:c.*334T>C	ENSP00000468912.1:n.*334T>C
ENST00000595952.5:c.*47T>C	ENSP00000471155.1:n.*47T>C
ENST00000596333.1:n.1011T>C
ENST00000598145.1:c.835T>C
ENST00000601349.5:n.2112T>C
ENST00000617027.4:c.*47T>C	ENSP00000483513.1:n.*47T>C
NM_001030047.1:c.*558T>C	NP_001025218.1:n.*558T>C
NM_001030048.1:c.*47T>C	NP_001025219.1:n.*47T>C
NM_001648.2:c.*47T>C MANE Select	NP_001639.1:n.*47T>C
XM_011526923.1:c.*47T>C	XP_011525225.1:n.*47T>C
XR_935817.1:n.1324+920T>C