Canonical Allele Identifier: CA979021098
Gene: RFWD3 HGNC NCBI

Linked Data

dbSNP Id: rs1959202682

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.74636615_74636619del , CM000678.2:g.74636615_74636619del GRCh38
NC_000016.9:g.74670513_74670517del , CM000678.1:g.74670513_74670517del GRCh37
NC_000016.8:g.73228014_73228018del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361070.9:c.1195-39_1195-35del MANE Select ENSP00000354361.4:n.1195-39_1195-35del
ENST00000361070.8:c.1195-39_1195-35del ENSP00000354361.4:n.1195-39_1195-35del
ENST00000571750.5:c.1195-39_1195-35del ENSP00000460049.1:n.1195-39_1195-35del
NM_018124.3:c.1195-39_1195-35del NP_060594.3:n.1195-39_1195-35del
XM_005256021.3:c.1195-39_1195-35del XP_005256078.1:n.1195-39_1195-35del
XM_005256022.3:c.1195-39_1195-35del XP_005256079.1:n.1195-39_1195-35del
XM_006721228.2:c.1195-39_1195-35del XP_006721291.1:n.1195-39_1195-35del
XM_011523191.1:c.1195-39_1195-35del XP_011521493.1:n.1195-39_1195-35del
XM_005256021.4:c.1195-39_1195-35del XP_005256078.1:n.1195-39_1195-35del
XM_005256022.4:c.1195-39_1195-35del XP_005256079.1:n.1195-39_1195-35del
XM_006721228.3:c.1195-39_1195-35del XP_006721291.1:n.1195-39_1195-35del
XM_011523191.3:c.1195-39_1195-35del XP_011521493.1:n.1195-39_1195-35del
XM_017023391.1:c.1195-39_1195-35del XP_016878880.1:n.1195-39_1195-35del
XM_017023392.1:c.1195-39_1195-35del XP_016878881.1:n.1195-39_1195-35del
NM_018124.4:c.1195-39_1195-35del MANE Select NP_060594.3:n.1195-39_1195-35del
NM_001370534.1:c.1195-39_1195-35del NP_001357463.1:n.1195-39_1195-35del
NM_001370535.1:c.1195-39_1195-35del NP_001357464.1:n.1195-39_1195-35del
NM_001370536.1:c.1195-39_1195-35del NP_001357465.1:n.1195-39_1195-35del
NM_001370537.1:c.361-39_361-35del NP_001357466.1:n.361-39_361-35del
NM_001370539.1:c.361-39_361-35del NP_001357468.1:n.361-39_361-35del
NM_001370540.1:c.361-39_361-35del NP_001357469.1:n.361-39_361-35del
NM_001370542.1:c.361-39_361-35del NP_001357471.1:n.361-39_361-35del
NM_001370543.1:c.361-39_361-35del NP_001357472.1:n.361-39_361-35del