Canonical Allele Identifier: CA407025260

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363376A>C (hg19) ; chr19:g.50860120A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860120A>C , CM000681.2:g.50860120A>C	GRCh38
NC_000019.9:g.51363376A>C , CM000681.1:g.51363376A>C	GRCh37
NC_000019.8:g.56055188A>C	NCBI36
NG_011653.1:g.10206A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.779A>C MANE Select	ENSP00000314151.1:p.Asn260Thr
ENST00000326003.6:c.779A>C	ENSP00000314151.1:p.Asn260Thr
ENST00000360617.7:c.1221A>C	ENSP00000353829.2:n.1221A>C
ENST00000422986.6:c.*435A>C	ENSP00000393628.2:n.*435A>C
ENST00000595392.5:c.*280A>C	ENSP00000468912.1:n.*280A>C
ENST00000595952.5:c.650A>C	ENSP00000471155.1:p.Asn217Thr
ENST00000596333.1:n.957A>C
ENST00000598145.1:c.781A>C
ENST00000601349.5:n.2058A>C
ENST00000601812.1:n.1211A>C
ENST00000617027.4:c.656A>C	ENSP00000483513.1:p.Asn219Thr
NM_001030047.1:c.*504A>C	NP_001025218.1:n.*504A>C
NM_001030048.1:c.650A>C	NP_001025219.1:p.Asn217Thr
NM_001648.2:c.779A>C MANE Select	NP_001639.1:p.Asn260Thr
XM_011526923.1:c.797A>C	XP_011525225.1:p.Asn266Thr
XR_935817.1:n.1324+866A>C