Canonical Allele Identifier: CA2586639304
Gene: KLK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50860420_50860421insTTC , CM000681.2:g.50860420_50860421insTTC GRCh38
NC_000019.9:g.51363676_51363677insTTC , CM000681.1:g.51363676_51363677insTTC GRCh37
NC_000019.8:g.56055488_56055489insTTC NCBI36
NG_011653.1:g.10506_10507insTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.*293_*294insTTC MANE Select ENSP00000314151.1:n.*293_*294insTTC
ENST00000326003.6:c.*293_*294insTTC ENSP00000314151.1:n.*293_*294insTTC
ENST00000360617.7:c.1521_1522insTTC ENSP00000353829.2:n.1521_1522insTTC
ENST00000422986.6:c.*735_*736insTTC ENSP00000393628.2:n.*735_*736insTTC
ENST00000595952.5:c.*293_*294insTTC ENSP00000471155.1:n.*293_*294insTTC
ENST00000596333.1:n.1257_1258insTTC
ENST00000601349.5:n.2358_2359insTTC
ENST00000617027.4:c.*293_*294insTTC ENSP00000483513.1:n.*293_*294insTTC
NM_001030047.1:c.*804_*805insTTC NP_001025218.1:n.*804_*805insTTC
NM_001030048.1:c.*293_*294insTTC NP_001025219.1:n.*293_*294insTTC
NM_001648.2:c.*293_*294insTTC MANE Select NP_001639.1:n.*293_*294insTTC
XM_011526923.1:c.*293_*294insTTC XP_011525225.1:n.*293_*294insTTC
XR_935817.1:n.1324+1166_1324+1167insTTC