Canonical Allele Identifier: CA2312018551
Gene: RTTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.70196639A= , CM000680.2:g.70196639A= GRCh38
NC_000018.9:g.67863875A= , CM000680.1:g.67863875A= GRCh37
NC_000018.8:g.66014855A= NCBI36
NG_033104.1:g.14088T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000255674.11:c.703T= ENSP00000255674.7:p.Ser235=
ENST00000638251.1:c.703T= ENSP00000491968.1:p.Ser235=
ENST00000640376.1:c.184T= ENSP00000491654.1:p.Ser62=
ENST00000640654.1:n.253T=
ENST00000640736.1:n.551T=
ENST00000640769.2:c.703T= MANE Select ENSP00000491507.1:p.Ser235=
ENST00000255674.10:c.703T= ENSP00000255674.6:p.Ser235=
ENST00000581161.5:c.703T= ENSP00000462926.1:p.Ser235=
ENST00000581583.1:n.771T=
ENST00000583043.5:c.73T= ENSP00000462733.1:p.Ser25=
NM_173630.3:c.703T= NP_775901.3:p.Ser235=
XM_005266679.1:c.-1851T= XP_005266736.1:n.-1851T=
XM_006722434.2:c.703T= XP_006722497.1:p.Ser235=
XM_006722435.2:c.703T= XP_006722498.1:p.Ser235=
XM_011525902.1:c.703T= XP_011524204.1:p.Ser235=
XM_011525903.1:c.703T= XP_011524205.1:p.Ser235=
XM_011525904.1:c.703T= XP_011524206.1:p.Ser235=
XM_011525905.1:c.703T= XP_011524207.1:p.Ser235=
XM_011525907.1:c.703T= XP_011524209.1:p.Ser235=
XM_011525908.1:c.703T= XP_011524210.1:p.Ser235=
XR_430072.2:n.741T=
XR_935213.1:n.741T=
NM_001318520.1:c.-1851T= NP_001305449.1:n.-1851T=
XM_006722434.3:c.703T= XP_006722497.1:p.Ser235=
XM_006722435.3:c.703T= XP_006722498.1:p.Ser235=
XM_011525902.2:c.703T= XP_011524204.1:p.Ser235=
XM_011525903.2:c.703T= XP_011524205.1:p.Ser235=
XM_011525904.3:c.703T= XP_011524206.1:p.Ser235=
XM_011525905.2:c.703T= XP_011524207.1:p.Ser235=
XM_011525907.2:c.703T= XP_011524209.1:p.Ser235=
XM_011525908.3:c.703T= XP_011524210.1:p.Ser235=
XM_017025693.1:c.703T= XP_016881182.1:p.Ser235=
XM_017025694.1:c.61T= XP_016881183.1:p.Ser21=
XM_017025696.1:c.-1469T= XP_016881185.1:n.-1469T=
XM_024451139.1:c.-78T= XP_024306907.1:n.-78T=
XM_024451140.1:c.-78T= XP_024306908.1:n.-78T=
XR_430072.3:n.771T=
XR_935213.2:n.771T=
NM_001318520.2:c.-1851T= NP_001305449.1:n.-1851T=
NM_173630.4:c.703T= MANE Select NP_775901.3:p.Ser235=