Canonical Allele Identifier: CA2311988306

Gene: RTTN

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.70127943_70127944delinsCT , CM000680.2:g.70127943_70127944delinsCT	GRCh38
NC_000018.9:g.67795179_67795180delinsCT , CM000680.1:g.67795179_67795180delinsCT	GRCh37
NC_000018.8:g.65946159_65946160delinsCT	NCBI36
NG_033104.1:g.82783_82784delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255674.11:c.3144-203_3144-202delinsAG	ENSP00000255674.7:n.3144-203_3144-202delinsAG
ENST00000638251.1:c.*1136-203_*1136-202delinsAG	ENSP00000491968.1:n.*1136-203_*1136-202delinsAG
ENST00000638298.1:c.132+110_132+111delinsAG
ENST00000639128.1:n.690-203_690-202delinsAG
ENST00000640376.1:c.2624+414_2624+415delinsAG	ENSP00000491654.1:n.2624+414_2624+415delinsAG
ENST00000640408.1:n.3576-203_3576-202delinsAG
ENST00000640769.2:c.3144-203_3144-202delinsAG MANE Select	ENSP00000491507.1:n.3144-203_3144-202delinsAG
ENST00000640931.1:c.365-203_365-202delinsAG
ENST00000677824.1:c.783-6244_783-6243delinsAG	ENSP00000504646.1:n.783-6244_783-6243delinsAG
ENST00000679113.1:c.366-203_366-202delinsAG	ENSP00000504487.1:n.366-203_366-202delinsAG
ENST00000255674.10:c.3144-203_3144-202delinsAG	ENSP00000255674.6:n.3144-203_3144-202delinsAG
ENST00000581161.5:c.*1458-203_*1458-202delinsAG	ENSP00000462926.1:n.*1458-203_*1458-202delinsAG
ENST00000583043.5:c.2425-203_2425-202delinsAG	ENSP00000462733.1:n.2425-203_2425-202delinsAG
NM_173630.3:c.3144-203_3144-202delinsAG	NP_775901.3:n.3144-203_3144-202delinsAG
XM_005266679.1:c.408-203_408-202delinsAG	XP_005266736.1:n.408-203_408-202delinsAG
XM_006722434.2:c.3147-203_3147-202delinsAG	XP_006722497.1:n.3147-203_3147-202delinsAG
XM_006722435.2:c.3147-203_3147-202delinsAG	XP_006722498.1:n.3147-203_3147-202delinsAG
XM_011525902.1:c.3146+414_3146+415delinsAG	XP_011524204.1:n.3146+414_3146+415delinsAG
XM_011525903.1:c.2958-6244_2958-6243delinsAG	XP_011524205.1:n.2958-6244_2958-6243delinsAG
XM_011525904.1:c.3147-203_3147-202delinsAG	XP_011524206.1:n.3147-203_3147-202delinsAG
XM_011525905.1:c.3147-203_3147-202delinsAG	XP_011524207.1:n.3147-203_3147-202delinsAG
XM_011525906.1:c.1647-203_1647-202delinsAG	XP_011524208.1:n.1647-203_1647-202delinsAG
XM_011525907.1:c.3147-203_3147-202delinsAG	XP_011524209.1:n.3147-203_3147-202delinsAG
XM_011525908.1:c.3147-203_3147-202delinsAG	XP_011524210.1:n.3147-203_3147-202delinsAG
XR_430072.2:n.3185-203_3185-202delinsAG
XR_935213.1:n.3185-203_3185-202delinsAG
NM_001318520.1:c.408-203_408-202delinsAG	NP_001305449.1:n.408-203_408-202delinsAG
XM_006722434.3:c.3147-203_3147-202delinsAG	XP_006722497.1:n.3147-203_3147-202delinsAG
XM_006722435.3:c.3147-203_3147-202delinsAG	XP_006722498.1:n.3147-203_3147-202delinsAG
XM_011525902.2:c.3146+414_3146+415delinsAG	XP_011524204.1:n.3146+414_3146+415delinsAG
XM_011525903.2:c.2958-6244_2958-6243delinsAG	XP_011524205.1:n.2958-6244_2958-6243delinsAG
XM_011525904.3:c.3147-203_3147-202delinsAG	XP_011524206.1:n.3147-203_3147-202delinsAG
XM_011525905.2:c.3147-203_3147-202delinsAG	XP_011524207.1:n.3147-203_3147-202delinsAG
XM_011525906.2:c.1647-203_1647-202delinsAG	XP_011524208.1:n.1647-203_1647-202delinsAG
XM_011525907.2:c.3147-203_3147-202delinsAG	XP_011524209.1:n.3147-203_3147-202delinsAG
XM_011525908.3:c.3147-203_3147-202delinsAG	XP_011524210.1:n.3147-203_3147-202delinsAG
XM_017025693.1:c.3143+414_3143+415delinsAG	XP_016881182.1:n.3143+414_3143+415delinsAG
XM_017025694.1:c.2505-203_2505-202delinsAG	XP_016881183.1:n.2505-203_2505-202delinsAG
XM_017025695.1:c.2082-203_2082-202delinsAG	XP_016881184.1:n.2082-203_2082-202delinsAG
XM_017025696.1:c.1038-203_1038-202delinsAG	XP_016881185.1:n.1038-203_1038-202delinsAG
XM_024451139.1:c.2367-203_2367-202delinsAG	XP_024306907.1:n.2367-203_2367-202delinsAG
XM_024451140.1:c.2367-203_2367-202delinsAG	XP_024306908.1:n.2367-203_2367-202delinsAG
XR_430072.3:n.3215-203_3215-202delinsAG
XR_935213.2:n.3215-203_3215-202delinsAG
NM_001318520.2:c.408-203_408-202delinsAG	NP_001305449.1:n.408-203_408-202delinsAG
NM_173630.4:c.3144-203_3144-202delinsAG MANE Select	NP_775901.3:n.3144-203_3144-202delinsAG