Canonical Allele Identifier: CA2311988350
Gene: RTTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.70128028A= , CM000680.2:g.70128028A= GRCh38
NC_000018.9:g.67795264A= , CM000680.1:g.67795264A= GRCh37
NC_000018.8:g.65946244A= NCBI36
NG_033104.1:g.82699T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000255674.11:c.3144-287T= ENSP00000255674.7:n.3144-287T=
ENST00000638251.1:c.*1136-287T= ENSP00000491968.1:n.*1136-287T=
ENST00000638298.1:c.132+26T=
ENST00000639128.1:n.690-287T=
ENST00000640376.1:c.2624+330T= ENSP00000491654.1:n.2624+330T=
ENST00000640408.1:n.3576-287T=
ENST00000640769.2:c.3144-287T= MANE Select ENSP00000491507.1:n.3144-287T=
ENST00000640931.1:c.365-287T=
ENST00000677824.1:c.783-6328T= ENSP00000504646.1:n.783-6328T=
ENST00000679113.1:c.366-287T= ENSP00000504487.1:n.366-287T=
ENST00000255674.10:c.3144-287T= ENSP00000255674.6:n.3144-287T=
ENST00000581161.5:c.*1458-287T= ENSP00000462926.1:n.*1458-287T=
ENST00000583043.5:c.2425-287T= ENSP00000462733.1:n.2425-287T=
NM_173630.3:c.3144-287T= NP_775901.3:n.3144-287T=
XM_005266679.1:c.408-287T= XP_005266736.1:n.408-287T=
XM_006722434.2:c.3147-287T= XP_006722497.1:n.3147-287T=
XM_006722435.2:c.3147-287T= XP_006722498.1:n.3147-287T=
XM_011525902.1:c.3146+330T= XP_011524204.1:n.3146+330T=
XM_011525903.1:c.2958-6328T= XP_011524205.1:n.2958-6328T=
XM_011525904.1:c.3147-287T= XP_011524206.1:n.3147-287T=
XM_011525905.1:c.3147-287T= XP_011524207.1:n.3147-287T=
XM_011525906.1:c.1647-287T= XP_011524208.1:n.1647-287T=
XM_011525907.1:c.3147-287T= XP_011524209.1:n.3147-287T=
XM_011525908.1:c.3147-287T= XP_011524210.1:n.3147-287T=
XR_430072.2:n.3185-287T=
XR_935213.1:n.3185-287T=
NM_001318520.1:c.408-287T= NP_001305449.1:n.408-287T=
XM_006722434.3:c.3147-287T= XP_006722497.1:n.3147-287T=
XM_006722435.3:c.3147-287T= XP_006722498.1:n.3147-287T=
XM_011525902.2:c.3146+330T= XP_011524204.1:n.3146+330T=
XM_011525903.2:c.2958-6328T= XP_011524205.1:n.2958-6328T=
XM_011525904.3:c.3147-287T= XP_011524206.1:n.3147-287T=
XM_011525905.2:c.3147-287T= XP_011524207.1:n.3147-287T=
XM_011525906.2:c.1647-287T= XP_011524208.1:n.1647-287T=
XM_011525907.2:c.3147-287T= XP_011524209.1:n.3147-287T=
XM_011525908.3:c.3147-287T= XP_011524210.1:n.3147-287T=
XM_017025693.1:c.3143+330T= XP_016881182.1:n.3143+330T=
XM_017025694.1:c.2505-287T= XP_016881183.1:n.2505-287T=
XM_017025695.1:c.2082-287T= XP_016881184.1:n.2082-287T=
XM_017025696.1:c.1038-287T= XP_016881185.1:n.1038-287T=
XM_024451139.1:c.2367-287T= XP_024306907.1:n.2367-287T=
XM_024451140.1:c.2367-287T= XP_024306908.1:n.2367-287T=
XR_430072.3:n.3215-287T=
XR_935213.2:n.3215-287T=
NM_001318520.2:c.408-287T= NP_001305449.1:n.408-287T=
NM_173630.4:c.3144-287T= MANE Select NP_775901.3:n.3144-287T=