Canonical Allele Identifier: CA1481580251

Gene: CISD2 SLC9B1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102885221G= , CM000666.2:g.102885221G=	GRCh38
NC_000004.11:g.103806378G= , CM000666.1:g.103806378G=	GRCh37
NC_000004.10:g.104025813G=	NCBI36
NG_008636.2:g.21244G=
NG_008662.2:g.139519C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273986.10:c.109G= (CISD2) MANE Select	ENSP00000273986.4:p.Glu37=
ENST00000643561.1:c.*91G= (CISD2)	ENSP00000494068.1:n.*91G=
ENST00000646632.1:c.*68G= (CISD2)	ENSP00000494257.1:n.*68G=
ENST00000273986.8:c.109G= (CISD2)	ENSP00000273986.4:p.Glu37=
ENST00000394789.7:c.*12C= (SLC9B1)	ENSP00000378269.3:n.*12C=
ENST00000503584.5:c.*952C= (SLC9B1)	ENSP00000426926.1:n.*952C=
ENST00000503643.1:c.139G= (CISD2)	ENSP00000423716.1:p.Glu47=
ENST00000514972.5:c.*709C= (SLC9B1)	ENSP00000426584.1:n.*709C=
ENST00000574446.1:c.*68G= (CISD2)	ENSP00000458976.1:n.*68G=
NM_001008388.4:c.109G= (CISD2)	NP_001008389.1:p.Glu37=
NM_001100874.2:c.*12C= (SLC9B1)	NP_001094344.1:n.*12C=
NR_047513.1:n.1454C= (SLC9B1)
NR_047515.1:n.1316C= (SLC9B1)
NM_001008388.5:c.109G= (CISD2) MANE Select	NP_001008389.1:p.Glu37=
NM_001100874.3:c.*12C= (SLC9B1)	NP_001094344.2:n.*12C=
NR_047513.2:n.1420C= (SLC9B1)
NR_047515.2:n.1282C= (SLC9B1)