Canonical Allele Identifier: CA920014338

Gene: RTTN

Linked Data

• dbSNP Id: rs575594450

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.70127979_70127986del , CM000680.2:g.70127979_70127986del	GRCh38
NC_000018.9:g.67795215_67795222del , CM000680.1:g.67795215_67795222del	GRCh37
NC_000018.8:g.65946195_65946202del	NCBI36
NG_033104.1:g.82744_82751del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255674.11:c.3144-242_3144-235del	ENSP00000255674.7:n.3144-242_3144-235del
ENST00000638251.1:c.*1136-242_*1136-235del	ENSP00000491968.1:n.*1136-242_*1136-235del
ENST00000638298.1:c.132+71_132+78del
ENST00000639128.1:n.690-242_690-235del
ENST00000640376.1:c.2624+375_2624+382del	ENSP00000491654.1:n.2624+375_2624+382del
ENST00000640408.1:n.3576-242_3576-235del
ENST00000640769.2:c.3144-242_3144-235del MANE Select	ENSP00000491507.1:n.3144-242_3144-235del
ENST00000640931.1:c.365-242_365-235del
ENST00000677824.1:c.783-6283_783-6276del	ENSP00000504646.1:n.783-6283_783-6276del
ENST00000679113.1:c.366-242_366-235del	ENSP00000504487.1:n.366-242_366-235del
ENST00000255674.10:c.3144-242_3144-235del	ENSP00000255674.6:n.3144-242_3144-235del
ENST00000581161.5:c.*1458-242_*1458-235del	ENSP00000462926.1:n.*1458-242_*1458-235del
ENST00000583043.5:c.2425-242_2425-235del	ENSP00000462733.1:n.2425-242_2425-235del
NM_173630.3:c.3144-242_3144-235del	NP_775901.3:n.3144-242_3144-235del
XM_005266679.1:c.408-242_408-235del	XP_005266736.1:n.408-242_408-235del
XM_006722434.2:c.3147-242_3147-235del	XP_006722497.1:n.3147-242_3147-235del
XM_006722435.2:c.3147-242_3147-235del	XP_006722498.1:n.3147-242_3147-235del
XM_011525902.1:c.3146+375_3146+382del	XP_011524204.1:n.3146+375_3146+382del
XM_011525903.1:c.2958-6283_2958-6276del	XP_011524205.1:n.2958-6283_2958-6276del
XM_011525904.1:c.3147-242_3147-235del	XP_011524206.1:n.3147-242_3147-235del
XM_011525905.1:c.3147-242_3147-235del	XP_011524207.1:n.3147-242_3147-235del
XM_011525906.1:c.1647-242_1647-235del	XP_011524208.1:n.1647-242_1647-235del
XM_011525907.1:c.3147-242_3147-235del	XP_011524209.1:n.3147-242_3147-235del
XM_011525908.1:c.3147-242_3147-235del	XP_011524210.1:n.3147-242_3147-235del
XR_430072.2:n.3185-242_3185-235del
XR_935213.1:n.3185-242_3185-235del
NM_001318520.1:c.408-242_408-235del	NP_001305449.1:n.408-242_408-235del
XM_006722434.3:c.3147-242_3147-235del	XP_006722497.1:n.3147-242_3147-235del
XM_006722435.3:c.3147-242_3147-235del	XP_006722498.1:n.3147-242_3147-235del
XM_011525902.2:c.3146+375_3146+382del	XP_011524204.1:n.3146+375_3146+382del
XM_011525903.2:c.2958-6283_2958-6276del	XP_011524205.1:n.2958-6283_2958-6276del
XM_011525904.3:c.3147-242_3147-235del	XP_011524206.1:n.3147-242_3147-235del
XM_011525905.2:c.3147-242_3147-235del	XP_011524207.1:n.3147-242_3147-235del
XM_011525906.2:c.1647-242_1647-235del	XP_011524208.1:n.1647-242_1647-235del
XM_011525907.2:c.3147-242_3147-235del	XP_011524209.1:n.3147-242_3147-235del
XM_011525908.3:c.3147-242_3147-235del	XP_011524210.1:n.3147-242_3147-235del
XM_017025693.1:c.3143+375_3143+382del	XP_016881182.1:n.3143+375_3143+382del
XM_017025694.1:c.2505-242_2505-235del	XP_016881183.1:n.2505-242_2505-235del
XM_017025695.1:c.2082-242_2082-235del	XP_016881184.1:n.2082-242_2082-235del
XM_017025696.1:c.1038-242_1038-235del	XP_016881185.1:n.1038-242_1038-235del
XM_024451139.1:c.2367-242_2367-235del	XP_024306907.1:n.2367-242_2367-235del
XM_024451140.1:c.2367-242_2367-235del	XP_024306908.1:n.2367-242_2367-235del
XR_430072.3:n.3215-242_3215-235del
XR_935213.2:n.3215-242_3215-235del
NM_001318520.2:c.408-242_408-235del	NP_001305449.1:n.408-242_408-235del
NM_173630.4:c.3144-242_3144-235del MANE Select	NP_775901.3:n.3144-242_3144-235del