Canonical Allele Identifier: CA2814740602

Gene: KLK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860425_50860426insCC , CM000681.2:g.50860425_50860426insCC	GRCh38
NC_000019.9:g.51363681_51363682insCC , CM000681.1:g.51363681_51363682insCC	GRCh37
NC_000019.8:g.56055493_56055494insCC	NCBI36
NG_011653.1:g.10511_10512insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.*298_*299insCC MANE Select	ENSP00000314151.1:n.*298_*299insCC
ENST00000326003.6:c.*298_*299insCC	ENSP00000314151.1:n.*298_*299insCC
ENST00000360617.7:c.1526_1527insCC	ENSP00000353829.2:n.1526_1527insCC
ENST00000422986.6:c.*740_*741insCC	ENSP00000393628.2:n.*740_*741insCC
ENST00000595952.5:c.*298_*299insCC	ENSP00000471155.1:n.*298_*299insCC
ENST00000596333.1:n.1262_1263insCC
ENST00000601349.5:n.2363_2364insCC
ENST00000617027.4:c.*298_*299insCC	ENSP00000483513.1:n.*298_*299insCC
NM_001030047.1:c.*809_*810insCC	NP_001025218.1:n.*809_*810insCC
NM_001030048.1:c.*298_*299insCC	NP_001025219.1:n.*298_*299insCC
NM_001648.2:c.*298_*299insCC MANE Select	NP_001639.1:n.*298_*299insCC
XM_011526923.1:c.*298_*299insCC	XP_011525225.1:n.*298_*299insCC
XR_935817.1:n.1324+1171_1324+1172insCC