Canonical Allele Identifier: CA2635153094
Gene: GEMIN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.745803_745805del , CM000679.2:g.745803_745805del GRCh38
NC_000017.10:g.649043_649045del , CM000679.1:g.649043_649045del GRCh37
NC_000017.9:g.595793_595795del NCBI36
NG_046938.1:g.12070_12072del

Transcript Alleles

HGVS Amino-acid change
ENST00000319004.6:c.2240_2242del MANE Select ENSP00000321706.5:p.Phe747del
ENST00000319004.5:c.2240_2242del ENSP00000321706.5:p.Phe747del
ENST00000576778.1:c.2207_2209del ENSP00000459565.1:p.Phe736del
NM_015721.2:c.2240_2242del NP_056536.2:p.Phe747del
XM_005256667.3:c.2252_2254del XP_005256724.1:p.Phe751del
XM_005256668.3:c.2252_2254del XP_005256725.1:p.Phe751del
XM_005256670.3:c.2207_2209del XP_005256727.1:p.Phe736del
XM_011523910.1:c.2252_2254del XP_011522212.1:p.Phe751del
XM_011523911.1:c.2252_2254del XP_011522213.1:p.Phe751del
XM_011523912.1:c.2207_2209del XP_011522214.1:p.Phe736del
XM_011523913.1:c.2207_2209del XP_011522215.1:p.Phe736del
XM_005256667.4:c.2252_2254del XP_005256724.1:p.Phe751del
XM_005256670.5:c.2207_2209del XP_005256727.1:p.Phe736del
XM_011523910.2:c.2252_2254del XP_011522212.1:p.Phe751del
XM_011523911.2:c.2252_2254del XP_011522213.1:p.Phe751del
XM_011523912.2:c.2207_2209del XP_011522214.1:p.Phe736del
XM_011523913.2:c.2207_2209del XP_011522215.1:p.Phe736del
XM_017024709.1:c.2252_2254del XP_016880198.1:p.Phe751del
NM_015721.3:c.2240_2242del MANE Select NP_056536.2:p.Phe747del