Canonical Allele Identifier: CA920129482

Gene: KLK3

Linked Data

• dbSNP Id: rs869273044

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50859727del , CM000681.2:g.50859727del	GRCh38
NC_000019.9:g.51362983del , CM000681.1:g.51362983del	GRCh37
NC_000019.8:g.56054795del	NCBI36
NG_011653.1:g.9813del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.631-245del MANE Select	ENSP00000314151.1:n.631-245del
ENST00000326003.6:c.631-245del	ENSP00000314151.1:n.631-245del
ENST00000360617.7:c.828del	ENSP00000353829.2:n.828del
ENST00000422986.6:c.*287-245del	ENSP00000393628.2:n.*287-245del
ENST00000595392.5:c.*132-245del	ENSP00000468912.1:n.*132-245del
ENST00000595952.5:c.502-245del	ENSP00000471155.1:n.502-245del
ENST00000596185.5:c.*739-245del	ENSP00000471648.1:n.*739-245del
ENST00000596333.1:n.809-245del
ENST00000597483.5:c.*111del	ENSP00000472411.1:n.*111del
ENST00000598145.1:c.633-245del
ENST00000601349.5:n.1910-245del
ENST00000601812.1:n.1063-245del
ENST00000617027.4:c.508-245del	ENSP00000483513.1:n.508-245del
NM_001030047.1:c.*111del	NP_001025218.1:n.*111del
NM_001030048.1:c.502-245del	NP_001025219.1:n.502-245del
NM_001648.2:c.631-245del MANE Select	NP_001639.1:n.631-245del
XM_011526923.1:c.649-245del	XP_011525225.1:n.649-245del
XM_011526924.1:c.*111del	XP_011525226.1:n.*111del
XR_935817.1:n.1324+473del