Canonical Allele Identifier: CA2576524749

Gene: RTTN

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.70059922_70059933del , CM000680.2:g.70059922_70059933del	GRCh38
NC_000018.9:g.67727158_67727169del , CM000680.1:g.67727158_67727169del	GRCh37
NC_000018.8:g.65878138_65878149del	NCBI36
NG_033104.1:g.150801_150812del

Transcript Alleles

HGVS	Amino-acid change
ENST00000255674.11:c.4864_4875del	ENSP00000255674.7:p.Asp1622_Leu1625del
ENST00000579986.6:c.951_962del	ENSP00000491518.1:p.Trp317Ter
ENST00000639128.1:n.2410_2421del
ENST00000639487.1:c.18_29del
ENST00000640769.2:c.4864_4875del MANE Select	ENSP00000491507.1:p.Asp1622_Leu1625del
ENST00000677824.1:c.2263_2274del	ENSP00000504646.1:p.Asp755_Leu758del
ENST00000679113.1:c.2216_2227del	ENSP00000504487.1:n.2216_2227del
ENST00000255674.10:c.4864_4875del	ENSP00000255674.6:p.Asp1622_Leu1625del
ENST00000581161.5:c.*3178_*3189del	ENSP00000462926.1:n.*3178_*3189del
ENST00000583043.5:c.4145_4156del	ENSP00000462733.1:n.4145_4156del
NM_173630.3:c.4864_4875del	NP_775901.3:p.Asp1622_Leu1625del
XM_005266679.1:c.2128_2139del	XP_005266736.1:p.Asp710_Leu713del
XM_006722434.2:c.4867_4878del	XP_006722497.1:p.Asp1623_Leu1626del
XM_006722435.2:c.4867_4878del	XP_006722498.1:p.Asp1623_Leu1626del
XM_011525902.1:c.4627_4638del	XP_011524204.1:p.Asp1543_Leu1546del
XM_011525903.1:c.4438_4449del	XP_011524205.1:p.Asp1480_Leu1483del
XM_011525904.1:c.4867_4878del	XP_011524206.1:p.Asp1623_Leu1626del
XM_011525905.1:c.4867_4878del	XP_011524207.1:p.Asp1623_Leu1626del
XM_011525906.1:c.3367_3378del	XP_011524208.1:p.Asp1123_Leu1126del
XR_430072.2:n.4905_4916del
NM_001318520.1:c.2128_2139del	NP_001305449.1:p.Asp710_Leu713del
XM_006722434.3:c.4867_4878del	XP_006722497.1:p.Asp1623_Leu1626del
XM_006722435.3:c.4867_4878del	XP_006722498.1:p.Asp1623_Leu1626del
XM_011525902.2:c.4627_4638del	XP_011524204.1:p.Asp1543_Leu1546del
XM_011525903.2:c.4438_4449del	XP_011524205.1:p.Asp1480_Leu1483del
XM_011525904.3:c.4867_4878del	XP_011524206.1:p.Asp1623_Leu1626del
XM_011525905.2:c.4867_4878del	XP_011524207.1:p.Asp1623_Leu1626del
XM_011525906.2:c.3367_3378del	XP_011524208.1:p.Asp1123_Leu1126del
XM_017025693.1:c.4624_4635del	XP_016881182.1:p.Asp1542_Leu1545del
XM_017025694.1:c.4225_4236del	XP_016881183.1:p.Asp1409_Leu1412del
XM_017025695.1:c.3802_3813del	XP_016881184.1:p.Asp1268_Leu1271del
XM_017025696.1:c.2758_2769del	XP_016881185.1:p.Asp920_Leu923del
XM_024451139.1:c.4087_4098del	XP_024306907.1:p.Asp1363_Leu1366del
XM_024451140.1:c.4087_4098del	XP_024306908.1:p.Asp1363_Leu1366del
XR_430072.3:n.4935_4946del
NM_001318520.2:c.2128_2139del	NP_001305449.1:p.Asp710_Leu713del
NM_173630.4:c.4864_4875del MANE Select	NP_775901.3:p.Asp1622_Leu1625del