Canonical Allele Identifier: CA427909897

Gene: RANBP2

Linked Data

• MyVariant Identifiers: chr2:g.109369938T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108753482T>C , CM000664.2:g.108753482T>C	GRCh38
NC_000002.11:g.109369938T>C , CM000664.1:g.109369938T>C	GRCh37
NC_000002.10:g.108736370T>C	NCBI36
NG_012210.1:g.39002T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697737.1:c.1974T>C	ENSP00000513426.1:p.Asp658=
ENST00000697740.1:c.1896T>C	ENSP00000513427.1:p.Asp632=
ENST00000283195.11:c.1974T>C MANE Select	ENSP00000283195.6:p.Asp658=
ENST00000283195.10:c.1974T>C	ENSP00000283195.6:p.Asp658=
NM_006267.4:c.1974T>C	NP_006258.3:p.Asp658=
XM_005264002.1:c.1974T>C	XP_005264059.1:p.Asp658=
XM_005264003.1:c.1974T>C	XP_005264060.1:p.Asp658=
XM_005264004.1:c.1974T>C	XP_005264061.1:p.Asp658=
XM_005264005.3:c.1896T>C	XP_005264062.1:p.Asp632=
XM_005264007.1:c.1974T>C	XP_005264064.1:p.Asp658=
XM_011511575.1:c.1971T>C	XP_011509877.1:p.Asp657=
XM_011511576.1:c.1974T>C	XP_011509878.1:p.Asp658=
XM_011511578.1:c.1971T>C	XP_011509880.1:p.Asp657=
XM_005264002.3:c.1974T>C	XP_005264059.1:p.Asp658=
XM_005264003.3:c.1974T>C	XP_005264060.1:p.Asp658=
XM_005264004.3:c.1974T>C	XP_005264061.1:p.Asp658=
XM_005264005.4:c.1896T>C	XP_005264062.1:p.Asp632=
XM_005264007.3:c.1974T>C	XP_005264064.1:p.Asp658=
XM_011511575.2:c.1971T>C	XP_011509877.1:p.Asp657=
XM_011511576.3:c.1974T>C	XP_011509878.1:p.Asp658=
XM_011511578.2:c.1971T>C	XP_011509880.1:p.Asp657=
XM_017004623.2:c.1974T>C	XP_016860112.1:p.Asp658=
XM_017004624.2:c.1974T>C	XP_016860113.1:p.Asp658=
XM_017004625.1:c.1974T>C	XP_016860114.1:p.Asp658=
NM_006267.5:c.1974T>C MANE Select	NP_006258.3:p.Asp658=