Canonical Allele Identifier: CA408966023

Gene: RIPOR3

Linked Data

• MyVariant Identifiers: chr20:g.49247296C>G (hg19) ; chr20:g.50630759C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.50630759C>G , CM000682.2:g.50630759C>G	GRCh38
NC_000020.10:g.49247296C>G , CM000682.1:g.49247296C>G	GRCh37
NC_000020.9:g.48680703C>G	NCBI36
NG_034040.1:g.65772G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327979.8:c.101G>C MANE Select	ENSP00000332663.3:p.Ser34Thr
ENST00000045083.6:c.89G>C	ENSP00000045083.2:p.Ser30Thr
ENST00000327979.6:c.89G>C	ENSP00000332663.2:p.Ser30Thr
ENST00000462493.1:n.407G>C
NM_001290268.1:c.101G>C	NP_001277197.1:p.Ser34Thr
NM_080829.3:c.89G>C	NP_543019.2:p.Ser30Thr
NR_110890.1:n.688G>C
XM_005260294.3:c.101G>C	XP_005260351.1:p.Ser34Thr
XM_006723713.2:c.101G>C	XP_006723776.1:p.Ser34Thr
XM_011528578.1:c.101G>C	XP_011526880.1:p.Ser34Thr
XM_011528579.1:c.89G>C	XP_011526881.1:p.Ser30Thr
XM_011528580.1:c.89G>C	XP_011526882.1:p.Ser30Thr
XM_011528581.1:c.89G>C	XP_011526883.1:p.Ser30Thr
XM_011528583.1:c.101G>C	XP_011526885.1:p.Ser34Thr
XM_011528584.1:c.101G>C	XP_011526886.1:p.Ser34Thr
XM_011528586.1:c.101G>C	XP_011526888.1:p.Ser34Thr
XR_936505.1:n.572G>C
XR_936506.1:n.573G>C
XM_006723713.4:c.101G>C	XP_006723776.1:p.Ser34Thr
XM_011528578.2:c.101G>C	XP_011526880.1:p.Ser34Thr
XM_011528579.2:c.89G>C	XP_011526881.1:p.Ser30Thr
XM_011528580.2:c.89G>C	XP_011526882.1:p.Ser30Thr
XM_011528581.2:c.89G>C	XP_011526883.1:p.Ser30Thr
XM_011528584.3:c.101G>C	XP_011526886.1:p.Ser34Thr
XM_011528586.2:c.101G>C	XP_011526888.1:p.Ser34Thr
XM_017027682.2:c.101G>C	XP_016883171.1:p.Ser34Thr
XR_001754183.1:n.565G>C
XR_936505.2:n.565G>C
XR_936506.3:n.566G>C
NM_001290268.2:c.101G>C MANE Select	NP_001277197.1:p.Ser34Thr
NR_110890.2:n.700G>C
NM_080829.4:c.89G>C	NP_543019.2:p.Ser30Thr