Canonical Allele Identifier: CA2311988231
Gene: RTTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.70127741T= , CM000680.2:g.70127741T= GRCh38
NC_000018.9:g.67794977T= , CM000680.1:g.67794977T= GRCh37
NC_000018.8:g.65945957T= NCBI36
NG_033104.1:g.82986A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000255674.11:c.3144A= ENSP00000255674.7:p.Glu1048=
ENST00000638251.1:c.*1136A= ENSP00000491968.1:n.*1136A=
ENST00000638298.1:c.133A=
ENST00000639128.1:n.690A=
ENST00000640376.1:c.2624+617A= ENSP00000491654.1:n.2624+617A=
ENST00000640408.1:n.3576A=
ENST00000640769.2:c.3144A= MANE Select ENSP00000491507.1:p.Glu1048=
ENST00000640931.1:c.365A=
ENST00000677824.1:c.783-6041A= ENSP00000504646.1:n.783-6041A=
ENST00000679113.1:c.366A= ENSP00000504487.1:p.Glu122=
ENST00000255674.10:c.3144A= ENSP00000255674.6:p.Glu1048=
ENST00000581161.5:c.*1458A= ENSP00000462926.1:n.*1458A=
ENST00000583043.5:c.2425A= ENSP00000462733.1:n.2425A=
NM_173630.3:c.3144A= NP_775901.3:p.Glu1048=
XM_005266679.1:c.408A= XP_005266736.1:p.Glu136=
XM_006722434.2:c.3147A= XP_006722497.1:p.Glu1049=
XM_006722435.2:c.3147A= XP_006722498.1:p.Glu1049=
XM_011525902.1:c.3146+617A= XP_011524204.1:n.3146+617A=
XM_011525903.1:c.2958-6041A= XP_011524205.1:n.2958-6041A=
XM_011525904.1:c.3147A= XP_011524206.1:p.Glu1049=
XM_011525905.1:c.3147A= XP_011524207.1:p.Glu1049=
XM_011525906.1:c.1647A= XP_011524208.1:p.Glu549=
XM_011525907.1:c.3147A= XP_011524209.1:p.Glu1049=
XM_011525908.1:c.3147A= XP_011524210.1:p.Glu1049=
XR_430072.2:n.3185A=
XR_935213.1:n.3185A=
NM_001318520.1:c.408A= NP_001305449.1:p.Glu136=
XM_006722434.3:c.3147A= XP_006722497.1:p.Glu1049=
XM_006722435.3:c.3147A= XP_006722498.1:p.Glu1049=
XM_011525902.2:c.3146+617A= XP_011524204.1:n.3146+617A=
XM_011525903.2:c.2958-6041A= XP_011524205.1:n.2958-6041A=
XM_011525904.3:c.3147A= XP_011524206.1:p.Glu1049=
XM_011525905.2:c.3147A= XP_011524207.1:p.Glu1049=
XM_011525906.2:c.1647A= XP_011524208.1:p.Glu549=
XM_011525907.2:c.3147A= XP_011524209.1:p.Glu1049=
XM_011525908.3:c.3147A= XP_011524210.1:p.Glu1049=
XM_017025693.1:c.3143+617A= XP_016881182.1:n.3143+617A=
XM_017025694.1:c.2505A= XP_016881183.1:p.Glu835=
XM_017025695.1:c.2082A= XP_016881184.1:p.Glu694=
XM_017025696.1:c.1038A= XP_016881185.1:p.Glu346=
XM_024451139.1:c.2367A= XP_024306907.1:p.Glu789=
XM_024451140.1:c.2367A= XP_024306908.1:p.Glu789=
XR_430072.3:n.3215A=
XR_935213.2:n.3215A=
NM_001318520.2:c.408A= NP_001305449.1:p.Glu136=
NM_173630.4:c.3144A= MANE Select NP_775901.3:p.Glu1048=