Canonical Allele Identifier: CA1481578503

Gene: CISD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102881008A= , CM000666.2:g.102881008A=	GRCh38
NC_000004.11:g.103802165A= , CM000666.1:g.103802165A=	GRCh37
NG_008636.2:g.17031A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273986.10:c.104-4208A= MANE Select	ENSP00000273986.4:n.104-4208A=
ENST00000643561.1:c.*86-4208A=	ENSP00000494068.1:n.*86-4208A=
ENST00000646632.1:c.104-1784A=	ENSP00000494257.1:n.104-1784A=
ENST00000273986.8:c.104-4208A=	ENSP00000273986.4:n.104-4208A=
ENST00000503643.1:c.134-4208A=	ENSP00000423716.1:n.134-4208A=
ENST00000574446.1:c.104-1763A=	ENSP00000458976.1:n.104-1763A=
NM_001008388.4:c.104-4208A=	NP_001008389.1:n.104-4208A=
NM_001008388.5:c.104-4208A= MANE Select	NP_001008389.1:n.104-4208A=