Canonical Allele Identifier: CA1822138
Gene: RANBP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 383037
dbSNP Id: rs138540027

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108740483T>C , CM000664.2:g.108740483T>C GRCh38
NC_000002.11:g.109356939T>C , CM000664.1:g.109356939T>C GRCh37
NC_000002.10:g.108723371T>C NCBI36
NG_012210.1:g.26003T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000697737.1:c.783-6T>C ENSP00000513426.1:n.783-6T>C
ENST00000697738.1:n.892-6T>C
ENST00000697739.1:n.817-6T>C
ENST00000697740.1:c.705-6T>C ENSP00000513427.1:n.705-6T>C
ENST00000283195.11:c.783-6T>C MANE Select ENSP00000283195.6:n.783-6T>C
ENST00000283195.10:c.783-6T>C ENSP00000283195.6:n.783-6T>C
NM_006267.4:c.783-6T>C NP_006258.3:n.783-6T>C
XM_005264002.1:c.783-6T>C XP_005264059.1:n.783-6T>C
XM_005264003.1:c.783-6T>C XP_005264060.1:n.783-6T>C
XM_005264004.1:c.783-6T>C XP_005264061.1:n.783-6T>C
XM_005264005.3:c.705-6T>C XP_005264062.1:n.705-6T>C
XM_005264007.1:c.783-6T>C XP_005264064.1:n.783-6T>C
XM_011511575.1:c.780-6T>C XP_011509877.1:n.780-6T>C
XM_011511576.1:c.783-6T>C XP_011509878.1:n.783-6T>C
XM_011511578.1:c.780-6T>C XP_011509880.1:n.780-6T>C
XM_005264002.3:c.783-6T>C XP_005264059.1:n.783-6T>C
XM_005264003.3:c.783-6T>C XP_005264060.1:n.783-6T>C
XM_005264004.3:c.783-6T>C XP_005264061.1:n.783-6T>C
XM_005264005.4:c.705-6T>C XP_005264062.1:n.705-6T>C
XM_005264007.3:c.783-6T>C XP_005264064.1:n.783-6T>C
XM_011511575.2:c.780-6T>C XP_011509877.1:n.780-6T>C
XM_011511576.3:c.783-6T>C XP_011509878.1:n.783-6T>C
XM_011511578.2:c.780-6T>C XP_011509880.1:n.780-6T>C
XM_017004623.2:c.783-6T>C XP_016860112.1:n.783-6T>C
XM_017004624.2:c.783-6T>C XP_016860113.1:n.783-6T>C
XM_017004625.1:c.783-6T>C XP_016860114.1:n.783-6T>C
NM_006267.5:c.783-6T>C MANE Select NP_006258.3:n.783-6T>C