Canonical Allele Identifier: CA2660603575

Gene: RANBP2

Linked Data

• gnomAD v4: 2-108768425-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108768425C>A , CM000664.2:g.108768425C>A	GRCh38
NC_000002.11:g.109384881C>A , CM000664.1:g.109384881C>A	GRCh37
NC_000002.10:g.108751313C>A	NCBI36
NG_012210.1:g.53945C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000697737.1:c.2603-3276C>A	ENSP00000513426.1:n.2603-3276C>A
ENST00000697740.1:c.2525-3276C>A	ENSP00000513427.1:n.2525-3276C>A
ENST00000697744.1:c.2715+37C>A
ENST00000697745.1:c.2715+37C>A
ENST00000697746.1:n.698C>A
ENST00000697747.1:c.480+37C>A
ENST00000697748.1:n.188C>A
ENST00000283195.11:c.7849+37C>A MANE Select	ENSP00000283195.6:n.7849+37C>A
ENST00000283195.10:c.7849+37C>A	ENSP00000283195.6:n.7849+37C>A
NM_006267.4:c.7849+37C>A	NP_006258.3:n.7849+37C>A
XM_005264002.1:c.7849+37C>A	XP_005264059.1:n.7849+37C>A
XM_005264003.1:c.7849+37C>A	XP_005264060.1:n.7849+37C>A
XM_005264004.1:c.7849+37C>A	XP_005264061.1:n.7849+37C>A
XM_005264005.3:c.7771+37C>A	XP_005264062.1:n.7771+37C>A
XM_005264007.1:c.4921+37C>A	XP_005264064.1:n.4921+37C>A
XM_011511575.1:c.7846+37C>A	XP_011509877.1:n.7846+37C>A
XM_011511576.1:c.7672+37C>A	XP_011509878.1:n.7672+37C>A
XM_011511577.1:c.5137+37C>A	XP_011509879.1:n.5137+37C>A
XM_011511578.1:c.4918+37C>A	XP_011509880.1:n.4918+37C>A
XM_005264002.3:c.7849+37C>A	XP_005264059.1:n.7849+37C>A
XM_005264003.3:c.7849+37C>A	XP_005264060.1:n.7849+37C>A
XM_005264004.3:c.7849+37C>A	XP_005264061.1:n.7849+37C>A
XM_005264005.4:c.7771+37C>A	XP_005264062.1:n.7771+37C>A
XM_005264007.3:c.4921+37C>A	XP_005264064.1:n.4921+37C>A
XM_011511575.2:c.7846+37C>A	XP_011509877.1:n.7846+37C>A
XM_011511576.3:c.7672+37C>A	XP_011509878.1:n.7672+37C>A
XM_011511578.2:c.4918+37C>A	XP_011509880.1:n.4918+37C>A
XM_017004623.2:c.7849+37C>A	XP_016860112.1:n.7849+37C>A
NM_006267.5:c.7849+37C>A MANE Select	NP_006258.3:n.7849+37C>A