Canonical Allele Identifier: CA2242474490
Gene: GEMIN4 HGNC NCBI

Linked Data

dbSNP Id: rs1974387054

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.745952_745954del , CM000679.2:g.745952_745954del GRCh38
NC_000017.10:g.649192_649194del , CM000679.1:g.649192_649194del GRCh37
NC_000017.9:g.595942_595944del NCBI36
NG_046938.1:g.11922_11924del

Transcript Alleles

HGVS Amino-acid Change
ENST00000319004.6:c.2092_2094del MANE Select ENSP00000321706.5:p.Leu698del
ENST00000319004.5:c.2092_2094del ENSP00000321706.5:p.Leu698del
ENST00000576778.1:c.2059_2061del ENSP00000459565.1:p.Leu687del
NM_015721.2:c.2092_2094del NP_056536.2:p.Leu698del
XM_005256667.3:c.2104_2106del XP_005256724.1:p.Leu702del
XM_005256668.3:c.2104_2106del XP_005256725.1:p.Leu702del
XM_005256670.3:c.2059_2061del XP_005256727.1:p.Leu687del
XM_011523910.1:c.2104_2106del XP_011522212.1:p.Leu702del
XM_011523911.1:c.2104_2106del XP_011522213.1:p.Leu702del
XM_011523912.1:c.2059_2061del XP_011522214.1:p.Leu687del
XM_011523913.1:c.2059_2061del XP_011522215.1:p.Leu687del
XM_005256667.4:c.2104_2106del XP_005256724.1:p.Leu702del
XM_005256670.5:c.2059_2061del XP_005256727.1:p.Leu687del
XM_011523910.2:c.2104_2106del XP_011522212.1:p.Leu702del
XM_011523911.2:c.2104_2106del XP_011522213.1:p.Leu702del
XM_011523912.2:c.2059_2061del XP_011522214.1:p.Leu687del
XM_011523913.2:c.2059_2061del XP_011522215.1:p.Leu687del
XM_017024709.1:c.2104_2106del XP_016880198.1:p.Leu702del
NM_015721.3:c.2092_2094del MANE Select NP_056536.2:p.Leu698del