Canonical Allele Identifier: CA407025195

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363356C>G (hg19) ; chr19:g.50860100C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860100C>G , CM000681.2:g.50860100C>G	GRCh38
NC_000019.9:g.51363356C>G , CM000681.1:g.51363356C>G	GRCh37
NC_000019.8:g.56055168C>G	NCBI36
NG_011653.1:g.10186C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.759C>G MANE Select	ENSP00000314151.1:p.Ile253Met
ENST00000326003.6:c.759C>G	ENSP00000314151.1:p.Ile253Met
ENST00000360617.7:c.1201C>G	ENSP00000353829.2:n.1201C>G
ENST00000422986.6:c.*415C>G	ENSP00000393628.2:n.*415C>G
ENST00000595392.5:c.*260C>G	ENSP00000468912.1:n.*260C>G
ENST00000595952.5:c.630C>G	ENSP00000471155.1:p.Ile210Met
ENST00000596333.1:n.937C>G
ENST00000598145.1:c.761C>G
ENST00000601349.5:n.2038C>G
ENST00000601812.1:n.1191C>G
ENST00000617027.4:c.636C>G	ENSP00000483513.1:p.Ile212Met
NM_001030047.1:c.*484C>G	NP_001025218.1:n.*484C>G
NM_001030048.1:c.630C>G	NP_001025219.1:p.Ile210Met
NM_001648.2:c.759C>G MANE Select	NP_001639.1:p.Ile253Met
XM_011526923.1:c.777C>G	XP_011525225.1:p.Ile259Met
XR_935817.1:n.1324+846C>G