Canonical Allele Identifier: CA366710683

Gene: RNF216

Linked Data

• MyVariant Identifiers: chr7:g.5680844G>T (hg19) ; chr7:g.5641213G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5641213G>T , CM000669.2:g.5641213G>T	GRCh38
NC_000007.13:g.5680844G>T , CM000669.1:g.5680844G>T	GRCh37
NC_000007.12:g.5647370G>T	NCBI36
NG_029374.1:g.145518C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389902.8:c.2323C>A MANE Select	ENSP00000374552.3:p.Arg775Ser
ENST00000389900.8:c.*1440C>A	ENSP00000374550.4:n.*1440C>A
ENST00000389902.7:c.2323C>A	ENSP00000374552.3:p.Arg775Ser
ENST00000425013.6:c.2152C>A	ENSP00000404602.2:p.Arg718Ser
ENST00000469375.1:n.540C>A
NM_207111.3:c.2323C>A	NP_996994.1:p.Arg775Ser
NM_207116.2:c.2152C>A	NP_996999.1:p.Arg718Ser
XM_005249785.2:c.2323C>A	XP_005249842.1:p.Arg775Ser
XM_006715748.1:c.1018C>A	XP_006715811.1:p.Arg340Ser
XM_011515434.1:c.2323C>A	XP_011513736.1:p.Arg775Ser
XM_011515436.1:c.1018C>A	XP_011513738.1:p.Arg340Ser
XM_011515436.2:c.1018C>A	XP_011513738.1:p.Arg340Ser
XM_017012363.2:c.2152C>A	XP_016867852.1:p.Arg718Ser
XM_024446805.1:c.2323C>A	XP_024302573.1:p.Arg775Ser
XM_024446806.1:c.1018C>A	XP_024302574.1:p.Arg340Ser
XM_024446807.1:c.1018C>A	XP_024302575.1:p.Arg340Ser
NM_001377156.1:c.2152C>A	NP_001364085.1:p.Arg718Ser
NM_207111.4:c.2323C>A MANE Select	NP_996994.1:p.Arg775Ser
NM_207116.3:c.2152C>A	NP_996999.1:p.Arg718Ser