Canonical Allele Identifier: CA2311988228
Gene: RTTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.70127735T= , CM000680.2:g.70127735T= GRCh38
NC_000018.9:g.67794971T= , CM000680.1:g.67794971T= GRCh37
NC_000018.8:g.65945951T= NCBI36
NG_033104.1:g.82992A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000255674.11:c.3150A= ENSP00000255674.7:p.Leu1050=
ENST00000638251.1:c.*1142A= ENSP00000491968.1:n.*1142A=
ENST00000638298.1:c.139A=
ENST00000639128.1:n.696A=
ENST00000640376.1:c.2624+623A= ENSP00000491654.1:n.2624+623A=
ENST00000640408.1:n.3582A=
ENST00000640769.2:c.3150A= MANE Select ENSP00000491507.1:p.Leu1050=
ENST00000640931.1:c.371A=
ENST00000677824.1:c.783-6035A= ENSP00000504646.1:n.783-6035A=
ENST00000679113.1:c.372A= ENSP00000504487.1:p.Leu124=
ENST00000255674.10:c.3150A= ENSP00000255674.6:p.Leu1050=
ENST00000581161.5:c.*1464A= ENSP00000462926.1:n.*1464A=
ENST00000583043.5:c.2431A= ENSP00000462733.1:n.2431A=
NM_173630.3:c.3150A= NP_775901.3:p.Leu1050=
XM_005266679.1:c.414A= XP_005266736.1:p.Leu138=
XM_006722434.2:c.3153A= XP_006722497.1:p.Leu1051=
XM_006722435.2:c.3153A= XP_006722498.1:p.Leu1051=
XM_011525902.1:c.3146+623A= XP_011524204.1:n.3146+623A=
XM_011525903.1:c.2958-6035A= XP_011524205.1:n.2958-6035A=
XM_011525904.1:c.3153A= XP_011524206.1:p.Leu1051=
XM_011525905.1:c.3153A= XP_011524207.1:p.Leu1051=
XM_011525906.1:c.1653A= XP_011524208.1:p.Leu551=
XM_011525907.1:c.3153A= XP_011524209.1:p.Leu1051=
XM_011525908.1:c.3153A= XP_011524210.1:p.Leu1051=
XR_430072.2:n.3191A=
XR_935213.1:n.3191A=
NM_001318520.1:c.414A= NP_001305449.1:p.Leu138=
XM_006722434.3:c.3153A= XP_006722497.1:p.Leu1051=
XM_006722435.3:c.3153A= XP_006722498.1:p.Leu1051=
XM_011525902.2:c.3146+623A= XP_011524204.1:n.3146+623A=
XM_011525903.2:c.2958-6035A= XP_011524205.1:n.2958-6035A=
XM_011525904.3:c.3153A= XP_011524206.1:p.Leu1051=
XM_011525905.2:c.3153A= XP_011524207.1:p.Leu1051=
XM_011525906.2:c.1653A= XP_011524208.1:p.Leu551=
XM_011525907.2:c.3153A= XP_011524209.1:p.Leu1051=
XM_011525908.3:c.3153A= XP_011524210.1:p.Leu1051=
XM_017025693.1:c.3143+623A= XP_016881182.1:n.3143+623A=
XM_017025694.1:c.2511A= XP_016881183.1:p.Leu837=
XM_017025695.1:c.2088A= XP_016881184.1:p.Leu696=
XM_017025696.1:c.1044A= XP_016881185.1:p.Leu348=
XM_024451139.1:c.2373A= XP_024306907.1:p.Leu791=
XM_024451140.1:c.2373A= XP_024306908.1:p.Leu791=
XR_430072.3:n.3221A=
XR_935213.2:n.3221A=
NM_001318520.2:c.414A= NP_001305449.1:p.Leu138=
NM_173630.4:c.3150A= MANE Select NP_775901.3:p.Leu1050=