Canonical Allele Identifier: CA2242476939

Gene: GEMIN4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.750578G= , CM000679.2:g.750578G=	GRCh38
NC_000017.10:g.653818G= , CM000679.1:g.653818G=	GRCh37
NC_000017.9:g.600568G=	NCBI36
NG_046938.1:g.7295C=

Transcript Alleles

HGVS	Amino-acid Change
NM_015721.3:c.10+1555C= MANE Select	NP_056536.2:n.10+1555C=
ENST00000319004.6:c.10+1555C= MANE Select	ENSP00000321706.5:n.10+1555C=
NM_015721.2:c.10+1555C=	NP_056536.2:n.10+1555C=
ENST00000319004.5:c.10+1555C=	ENSP00000321706.5:n.10+1555C=
ENST00000437269.1:c.10+1555C=	ENSP00000392460.1:n.10+1555C=
ENST00000570364.5:c.-74-669C=	ENSP00000461103.1:n.-74-669C=
ENST00000573482.5:c.-74-669C=	ENSP00000460286.1:n.-74-669C=
ENST00000574958.1:c.-74-669C=	ENSP00000458896.1:n.-74-669C=
ENST00000576383.1:c.-23-2546C=	ENSP00000461368.1:n.-23-2546C=
XM_005256667.3:c.-74-669C=	XP_005256724.1:n.-74-669C=
XM_005256667.4:c.-74-669C=	XP_005256724.1:n.-74-669C=
XM_005256670.3:c.-24+2040C=	XP_005256727.1:n.-24+2040C=
XM_005256670.5:c.-24+2040C=	XP_005256727.1:n.-24+2040C=
XM_011523910.1:c.-74-669C=	XP_011522212.1:n.-74-669C=
XM_011523910.2:c.-74-669C=	XP_011522212.1:n.-74-669C=
XM_011523911.1:c.-74-669C=	XP_011522213.1:n.-74-669C=
XM_011523911.2:c.-74-669C=	XP_011522213.1:n.-74-669C=
XM_011523912.1:c.-605C=	XP_011522214.1:n.-605C=
XM_011523912.2:c.-605C=	XP_011522214.1:n.-605C=
XM_011523913.1:c.-24+1073C=	XP_011522215.1:n.-24+1073C=
XM_011523913.2:c.-24+1073C=	XP_011522215.1:n.-24+1073C=
XM_017024709.1:c.-326-330C=	XP_016880198.1:n.-326-330C=