Canonical Allele Identifier: CA2311988210
Gene: RTTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.70127702_70127703delinsGA , CM000680.2:g.70127702_70127703delinsGA GRCh38
NC_000018.9:g.67794938_67794939delinsGA , CM000680.1:g.67794938_67794939delinsGA GRCh37
NC_000018.8:g.65945918_65945919delinsGA NCBI36
NG_033104.1:g.83024_83025delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000255674.11:c.3182_3183delinsTC ENSP00000255674.7:p.Leu1061=
ENST00000638251.1:c.*1174_*1175delinsTC ENSP00000491968.1:n.*1174_*1175delinsTC
ENST00000638298.1:c.171_172delinsTC
ENST00000639128.1:n.728_729delinsTC
ENST00000640376.1:c.2624+655_2624+656delinsTC ENSP00000491654.1:n.2624+655_2624+656delinsTC
ENST00000640408.1:n.3614_3615delinsTC
ENST00000640769.2:c.3182_3183delinsTC MANE Select ENSP00000491507.1:p.Leu1061=
ENST00000640931.1:c.403_404delinsTC
ENST00000677824.1:c.783-6003_783-6002delinsTC ENSP00000504646.1:n.783-6003_783-6002delinsTC
ENST00000679113.1:c.404_405delinsTC ENSP00000504487.1:p.Leu135=
ENST00000255674.10:c.3182_3183delinsTC ENSP00000255674.6:p.Leu1061=
ENST00000581161.5:c.*1496_*1497delinsTC ENSP00000462926.1:n.*1496_*1497delinsTC
ENST00000583043.5:c.2463_2464delinsTC ENSP00000462733.1:n.2463_2464delinsTC
NM_173630.3:c.3182_3183delinsTC NP_775901.3:p.Leu1061=
XM_005266679.1:c.446_447delinsTC XP_005266736.1:p.Leu149=
XM_006722434.2:c.3185_3186delinsTC XP_006722497.1:p.Leu1062=
XM_006722435.2:c.3185_3186delinsTC XP_006722498.1:p.Leu1062=
XM_011525902.1:c.3146+655_3146+656delinsTC XP_011524204.1:n.3146+655_3146+656delinsTC
XM_011525903.1:c.2958-6003_2958-6002delinsTC XP_011524205.1:n.2958-6003_2958-6002delinsTC
XM_011525904.1:c.3185_3186delinsTC XP_011524206.1:p.Leu1062=
XM_011525905.1:c.3185_3186delinsTC XP_011524207.1:p.Leu1062=
XM_011525906.1:c.1685_1686delinsTC XP_011524208.1:p.Leu562=
XM_011525907.1:c.3185_3186delinsTC XP_011524209.1:p.Leu1062=
XM_011525908.1:c.3185_3186delinsTC XP_011524210.1:p.Leu1062=
XR_430072.2:n.3223_3224delinsTC
XR_935213.1:n.3223_3224delinsTC
NM_001318520.1:c.446_447delinsTC NP_001305449.1:p.Leu149=
XM_006722434.3:c.3185_3186delinsTC XP_006722497.1:p.Leu1062=
XM_006722435.3:c.3185_3186delinsTC XP_006722498.1:p.Leu1062=
XM_011525902.2:c.3146+655_3146+656delinsTC XP_011524204.1:n.3146+655_3146+656delinsTC
XM_011525903.2:c.2958-6003_2958-6002delinsTC XP_011524205.1:n.2958-6003_2958-6002delinsTC
XM_011525904.3:c.3185_3186delinsTC XP_011524206.1:p.Leu1062=
XM_011525905.2:c.3185_3186delinsTC XP_011524207.1:p.Leu1062=
XM_011525906.2:c.1685_1686delinsTC XP_011524208.1:p.Leu562=
XM_011525907.2:c.3185_3186delinsTC XP_011524209.1:p.Leu1062=
XM_011525908.3:c.3185_3186delinsTC XP_011524210.1:p.Leu1062=
XM_017025693.1:c.3143+655_3143+656delinsTC XP_016881182.1:n.3143+655_3143+656delinsTC
XM_017025694.1:c.2543_2544delinsTC XP_016881183.1:p.Leu848=
XM_017025695.1:c.2120_2121delinsTC XP_016881184.1:p.Leu707=
XM_017025696.1:c.1076_1077delinsTC XP_016881185.1:p.Leu359=
XM_024451139.1:c.2405_2406delinsTC XP_024306907.1:p.Leu802=
XM_024451140.1:c.2405_2406delinsTC XP_024306908.1:p.Leu802=
XR_430072.3:n.3253_3254delinsTC
XR_935213.2:n.3253_3254delinsTC
NM_001318520.2:c.446_447delinsTC NP_001305449.1:p.Leu149=
NM_173630.4:c.3182_3183delinsTC MANE Select NP_775901.3:p.Leu1061=