Canonical Allele Identifier: CA402694301

Gene: RTTN

Linked Data

• MyVariant Identifiers: chr18:g.67727110G>C (hg19) ; chr18:g.70059874G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.70059874G>C , CM000680.2:g.70059874G>C	GRCh38
NC_000018.9:g.67727110G>C , CM000680.1:g.67727110G>C	GRCh37
NC_000018.8:g.65878090G>C	NCBI36
NG_033104.1:g.150853C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255674.11:c.4916C>G	ENSP00000255674.7:p.Ala1639Gly
ENST00000579986.6:c.1003C>G	ENSP00000491518.1:n.1003C>G
ENST00000639128.1:n.2462C>G
ENST00000639487.1:c.70C>G
ENST00000640769.2:c.4916C>G MANE Select	ENSP00000491507.1:p.Ala1639Gly
ENST00000677824.1:c.2315C>G	ENSP00000504646.1:p.Ala772Gly
ENST00000679113.1:c.2268C>G	ENSP00000504487.1:n.2268C>G
ENST00000255674.10:c.4916C>G	ENSP00000255674.6:p.Ala1639Gly
ENST00000581161.5:c.*3230C>G	ENSP00000462926.1:n.*3230C>G
ENST00000583043.5:c.4197C>G	ENSP00000462733.1:n.4197C>G
NM_173630.3:c.4916C>G	NP_775901.3:p.Ala1639Gly
XM_005266679.1:c.2180C>G	XP_005266736.1:p.Ala727Gly
XM_006722434.2:c.4919C>G	XP_006722497.1:p.Ala1640Gly
XM_006722435.2:c.4919C>G	XP_006722498.1:p.Ala1640Gly
XM_011525902.1:c.4679C>G	XP_011524204.1:p.Ala1560Gly
XM_011525903.1:c.4490C>G	XP_011524205.1:p.Ala1497Gly
XM_011525904.1:c.4919C>G	XP_011524206.1:p.Ala1640Gly
XM_011525905.1:c.4919C>G	XP_011524207.1:p.Ala1640Gly
XM_011525906.1:c.3419C>G	XP_011524208.1:p.Ala1140Gly
XR_430072.2:n.4957C>G
NM_001318520.1:c.2180C>G	NP_001305449.1:p.Ala727Gly
XM_006722434.3:c.4919C>G	XP_006722497.1:p.Ala1640Gly
XM_006722435.3:c.4919C>G	XP_006722498.1:p.Ala1640Gly
XM_011525902.2:c.4679C>G	XP_011524204.1:p.Ala1560Gly
XM_011525903.2:c.4490C>G	XP_011524205.1:p.Ala1497Gly
XM_011525904.3:c.4919C>G	XP_011524206.1:p.Ala1640Gly
XM_011525905.2:c.4919C>G	XP_011524207.1:p.Ala1640Gly
XM_011525906.2:c.3419C>G	XP_011524208.1:p.Ala1140Gly
XM_017025693.1:c.4676C>G	XP_016881182.1:p.Ala1559Gly
XM_017025694.1:c.4277C>G	XP_016881183.1:p.Ala1426Gly
XM_017025695.1:c.3854C>G	XP_016881184.1:p.Ala1285Gly
XM_017025696.1:c.2810C>G	XP_016881185.1:p.Ala937Gly
XM_024451139.1:c.4139C>G	XP_024306907.1:p.Ala1380Gly
XM_024451140.1:c.4139C>G	XP_024306908.1:p.Ala1380Gly
XR_430072.3:n.4987C>G
NM_001318520.2:c.2180C>G	NP_001305449.1:p.Ala727Gly
NM_173630.4:c.4916C>G MANE Select	NP_775901.3:p.Ala1639Gly