Canonical Allele Identifier: CA2242474489

Gene: GEMIN4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.745948_745951delinsAGAG , CM000679.2:g.745948_745951delinsAGAG	GRCh38
NC_000017.10:g.649188_649191delinsAGAG , CM000679.1:g.649188_649191delinsAGAG	GRCh37
NC_000017.9:g.595938_595941delinsAGAG	NCBI36
NG_046938.1:g.11922_11925delinsCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319004.6:c.2092_2095delinsCTCT MANE Select	ENSP00000321706.5:p.Leu698=
ENST00000319004.5:c.2092_2095delinsCTCT	ENSP00000321706.5:p.Leu698=
ENST00000576778.1:c.2059_2062delinsCTCT	ENSP00000459565.1:p.Leu687=
NM_015721.2:c.2092_2095delinsCTCT	NP_056536.2:p.Leu698=
XM_005256667.3:c.2104_2107delinsCTCT	XP_005256724.1:p.Leu702=
XM_005256668.3:c.2104_2107delinsCTCT	XP_005256725.1:p.Leu702=
XM_005256670.3:c.2059_2062delinsCTCT	XP_005256727.1:p.Leu687=
XM_011523910.1:c.2104_2107delinsCTCT	XP_011522212.1:p.Leu702=
XM_011523911.1:c.2104_2107delinsCTCT	XP_011522213.1:p.Leu702=
XM_011523912.1:c.2059_2062delinsCTCT	XP_011522214.1:p.Leu687=
XM_011523913.1:c.2059_2062delinsCTCT	XP_011522215.1:p.Leu687=
XM_005256667.4:c.2104_2107delinsCTCT	XP_005256724.1:p.Leu702=
XM_005256670.5:c.2059_2062delinsCTCT	XP_005256727.1:p.Leu687=
XM_011523910.2:c.2104_2107delinsCTCT	XP_011522212.1:p.Leu702=
XM_011523911.2:c.2104_2107delinsCTCT	XP_011522213.1:p.Leu702=
XM_011523912.2:c.2059_2062delinsCTCT	XP_011522214.1:p.Leu687=
XM_011523913.2:c.2059_2062delinsCTCT	XP_011522215.1:p.Leu687=
XM_017024709.1:c.2104_2107delinsCTCT	XP_016880198.1:p.Leu702=
NM_015721.3:c.2092_2095delinsCTCT MANE Select	NP_056536.2:p.Leu698=