Canonical Allele Identifier: CA2576867272

Gene: KLK3

Linked Data

• gnomAD v4: 19-50860156-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860156A>C , CM000681.2:g.50860156A>C	GRCh38
NC_000019.9:g.51363412A>C , CM000681.1:g.51363412A>C	GRCh37
NC_000019.8:g.56055224A>C	NCBI36
NG_011653.1:g.10242A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.*29A>C MANE Select	ENSP00000314151.1:n.*29A>C
ENST00000326003.6:c.*29A>C	ENSP00000314151.1:n.*29A>C
ENST00000360617.7:c.1257A>C	ENSP00000353829.2:n.1257A>C
ENST00000422986.6:c.*471A>C	ENSP00000393628.2:n.*471A>C
ENST00000595392.5:c.*316A>C	ENSP00000468912.1:n.*316A>C
ENST00000595952.5:c.*29A>C	ENSP00000471155.1:n.*29A>C
ENST00000596333.1:n.993A>C
ENST00000598145.1:c.817A>C
ENST00000601349.5:n.2094A>C
ENST00000617027.4:c.*29A>C	ENSP00000483513.1:n.*29A>C
NM_001030047.1:c.*540A>C	NP_001025218.1:n.*540A>C
NM_001030048.1:c.*29A>C	NP_001025219.1:n.*29A>C
NM_001648.2:c.*29A>C MANE Select	NP_001639.1:n.*29A>C
XM_011526923.1:c.*29A>C	XP_011525225.1:n.*29A>C
XR_935817.1:n.1324+902A>C