Canonical Allele Identifier: CA2311988209
Gene: RTTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.70127695_70127697delinsTCA , CM000680.2:g.70127695_70127697delinsTCA GRCh38
NC_000018.9:g.67794931_67794933delinsTCA , CM000680.1:g.67794931_67794933delinsTCA GRCh37
NC_000018.8:g.65945911_65945913delinsTCA NCBI36
NG_033104.1:g.83030_83032delinsTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000255674.11:c.3188_3190delinsTGA ENSP00000255674.7:p.Leu1063=
ENST00000638251.1:c.*1180_*1182delinsTGA ENSP00000491968.1:n.*1180_*1182delinsTGA
ENST00000638298.1:c.177_179delinsTGA
ENST00000639128.1:n.734_736delinsTGA
ENST00000640376.1:c.2624+661_2624+663delinsTGA ENSP00000491654.1:n.2624+661_2624+663delinsTGA
ENST00000640408.1:n.3620_3622delinsTGA
ENST00000640769.2:c.3188_3190delinsTGA MANE Select ENSP00000491507.1:p.Leu1063=
ENST00000640931.1:c.409_411delinsTGA
ENST00000677824.1:c.783-5997_783-5995delinsTGA ENSP00000504646.1:n.783-5997_783-5995delinsTGA
ENST00000679113.1:c.410_412delinsTGA ENSP00000504487.1:p.Leu137=
ENST00000255674.10:c.3188_3190delinsTGA ENSP00000255674.6:p.Leu1063=
ENST00000581161.5:c.*1502_*1504delinsTGA ENSP00000462926.1:n.*1502_*1504delinsTGA
ENST00000583043.5:c.2469_2471delinsTGA ENSP00000462733.1:n.2469_2471delinsTGA
NM_173630.3:c.3188_3190delinsTGA NP_775901.3:p.Leu1063=
XM_005266679.1:c.452_454delinsTGA XP_005266736.1:p.Leu151=
XM_006722434.2:c.3191_3193delinsTGA XP_006722497.1:p.Leu1064=
XM_006722435.2:c.3191_3193delinsTGA XP_006722498.1:p.Leu1064=
XM_011525902.1:c.3146+661_3146+663delinsTGA XP_011524204.1:n.3146+661_3146+663delinsTGA
XM_011525903.1:c.2958-5997_2958-5995delinsTGA XP_011524205.1:n.2958-5997_2958-5995delinsTGA
XM_011525904.1:c.3191_3193delinsTGA XP_011524206.1:p.Leu1064=
XM_011525905.1:c.3191_3193delinsTGA XP_011524207.1:p.Leu1064=
XM_011525906.1:c.1691_1693delinsTGA XP_011524208.1:p.Leu564=
XM_011525907.1:c.3191_3193delinsTGA XP_011524209.1:p.Leu1064=
XM_011525908.1:c.3191_3193delinsTGA XP_011524210.1:p.Leu1064=
XR_430072.2:n.3229_3231delinsTGA
XR_935213.1:n.3229_3231delinsTGA
NM_001318520.1:c.452_454delinsTGA NP_001305449.1:p.Leu151=
XM_006722434.3:c.3191_3193delinsTGA XP_006722497.1:p.Leu1064=
XM_006722435.3:c.3191_3193delinsTGA XP_006722498.1:p.Leu1064=
XM_011525902.2:c.3146+661_3146+663delinsTGA XP_011524204.1:n.3146+661_3146+663delinsTGA
XM_011525903.2:c.2958-5997_2958-5995delinsTGA XP_011524205.1:n.2958-5997_2958-5995delinsTGA
XM_011525904.3:c.3191_3193delinsTGA XP_011524206.1:p.Leu1064=
XM_011525905.2:c.3191_3193delinsTGA XP_011524207.1:p.Leu1064=
XM_011525906.2:c.1691_1693delinsTGA XP_011524208.1:p.Leu564=
XM_011525907.2:c.3191_3193delinsTGA XP_011524209.1:p.Leu1064=
XM_011525908.3:c.3191_3193delinsTGA XP_011524210.1:p.Leu1064=
XM_017025693.1:c.3143+661_3143+663delinsTGA XP_016881182.1:n.3143+661_3143+663delinsTGA
XM_017025694.1:c.2549_2551delinsTGA XP_016881183.1:p.Leu850=
XM_017025695.1:c.2126_2128delinsTGA XP_016881184.1:p.Leu709=
XM_017025696.1:c.1082_1084delinsTGA XP_016881185.1:p.Leu361=
XM_024451139.1:c.2411_2413delinsTGA XP_024306907.1:p.Leu804=
XM_024451140.1:c.2411_2413delinsTGA XP_024306908.1:p.Leu804=
XR_430072.3:n.3259_3261delinsTGA
XR_935213.2:n.3259_3261delinsTGA
NM_001318520.2:c.452_454delinsTGA NP_001305449.1:p.Leu151=
NM_173630.4:c.3188_3190delinsTGA MANE Select NP_775901.3:p.Leu1063=