Canonical Allele Identifier: CA348053121

Gene: RANBP2

Linked Data

• ClinVar Variation Id: 1416151
• ClinVar RCV Id: RCV001935554
• dbSNP Id: rs1676066238
• MyVariant Identifiers: chr2:g.109369939G>T (hg19) ; chr2:g.108753483G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108753483G>T , CM000664.2:g.108753483G>T	GRCh38
NC_000002.11:g.109369939G>T , CM000664.1:g.109369939G>T	GRCh37
NC_000002.10:g.108736371G>T	NCBI36
NG_012210.1:g.39003G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697737.1:c.1975G>T	ENSP00000513426.1:p.Ala659Ser
ENST00000697740.1:c.1897G>T	ENSP00000513427.1:p.Ala633Ser
ENST00000283195.11:c.1975G>T MANE Select	ENSP00000283195.6:p.Ala659Ser
ENST00000283195.10:c.1975G>T	ENSP00000283195.6:p.Ala659Ser
NM_006267.4:c.1975G>T	NP_006258.3:p.Ala659Ser
XM_005264002.1:c.1975G>T	XP_005264059.1:p.Ala659Ser
XM_005264003.1:c.1975G>T	XP_005264060.1:p.Ala659Ser
XM_005264004.1:c.1975G>T	XP_005264061.1:p.Ala659Ser
XM_005264005.3:c.1897G>T	XP_005264062.1:p.Ala633Ser
XM_005264007.1:c.1975G>T	XP_005264064.1:p.Ala659Ser
XM_011511575.1:c.1972G>T	XP_011509877.1:p.Ala658Ser
XM_011511576.1:c.1975G>T	XP_011509878.1:p.Ala659Ser
XM_011511578.1:c.1972G>T	XP_011509880.1:p.Ala658Ser
XM_005264002.3:c.1975G>T	XP_005264059.1:p.Ala659Ser
XM_005264003.3:c.1975G>T	XP_005264060.1:p.Ala659Ser
XM_005264004.3:c.1975G>T	XP_005264061.1:p.Ala659Ser
XM_005264005.4:c.1897G>T	XP_005264062.1:p.Ala633Ser
XM_005264007.3:c.1975G>T	XP_005264064.1:p.Ala659Ser
XM_011511575.2:c.1972G>T	XP_011509877.1:p.Ala658Ser
XM_011511576.3:c.1975G>T	XP_011509878.1:p.Ala659Ser
XM_011511578.2:c.1972G>T	XP_011509880.1:p.Ala658Ser
XM_017004623.2:c.1975G>T	XP_016860112.1:p.Ala659Ser
XM_017004624.2:c.1975G>T	XP_016860113.1:p.Ala659Ser
XM_017004625.1:c.1975G>T	XP_016860114.1:p.Ala659Ser
NM_006267.5:c.1975G>T MANE Select	NP_006258.3:p.Ala659Ser