Canonical Allele Identifier: CA348082193

Gene: RANBP2

Linked Data

• MyVariant Identifiers: chr2:g.109388218A>C (hg19) ; chr2:g.108771762A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108771762A>C , CM000664.2:g.108771762A>C	GRCh38
NC_000002.11:g.109388218A>C , CM000664.1:g.109388218A>C	GRCh37
NC_000002.10:g.108754650A>C	NCBI36
NG_012210.1:g.57282A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697737.1:c.2664A>C	ENSP00000513426.1:p.Glu888Asp
ENST00000697740.1:c.2586A>C	ENSP00000513427.1:p.Glu862Asp
ENST00000697744.1:c.2777A>C
ENST00000697745.1:c.2777A>C
ENST00000697746.1:n.4035A>C
ENST00000697747.1:c.620A>C
ENST00000697748.1:n.3525A>C
ENST00000283195.11:c.7911A>C MANE Select	ENSP00000283195.6:p.Glu2637Asp
ENST00000283195.10:c.7911A>C	ENSP00000283195.6:p.Glu2637Asp
NM_006267.4:c.7911A>C	NP_006258.3:p.Glu2637Asp
XM_005264002.1:c.7989A>C	XP_005264059.1:p.Glu2663Asp
XM_005264003.1:c.7989A>C	XP_005264060.1:p.Glu2663Asp
XM_005264004.1:c.7911A>C	XP_005264061.1:p.Glu2637Asp
XM_005264005.3:c.7911A>C	XP_005264062.1:p.Glu2637Asp
XM_005264007.1:c.5061A>C	XP_005264064.1:p.Glu1687Asp
XM_011511575.1:c.7986A>C	XP_011509877.1:p.Glu2662Asp
XM_011511576.1:c.7812A>C	XP_011509878.1:p.Glu2604Asp
XM_011511577.1:c.5277A>C	XP_011509879.1:p.Glu1759Asp
XM_011511578.1:c.5058A>C	XP_011509880.1:p.Glu1686Asp
XM_005264002.3:c.7989A>C	XP_005264059.1:p.Glu2663Asp
XM_005264003.3:c.7989A>C	XP_005264060.1:p.Glu2663Asp
XM_005264004.3:c.7911A>C	XP_005264061.1:p.Glu2637Asp
XM_005264005.4:c.7911A>C	XP_005264062.1:p.Glu2637Asp
XM_005264007.3:c.5061A>C	XP_005264064.1:p.Glu1687Asp
XM_011511575.2:c.7986A>C	XP_011509877.1:p.Glu2662Asp
XM_011511576.3:c.7812A>C	XP_011509878.1:p.Glu2604Asp
XM_011511578.2:c.5058A>C	XP_011509880.1:p.Glu1686Asp
XM_017004623.2:c.7989A>C	XP_016860112.1:p.Glu2663Asp
NM_006267.5:c.7911A>C MANE Select	NP_006258.3:p.Glu2637Asp