Canonical Allele Identifier: CA2311988222

Gene: RTTN

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.70127723_70127725delinsCTT , CM000680.2:g.70127723_70127725delinsCTT	GRCh38
NC_000018.9:g.67794959_67794961delinsCTT , CM000680.1:g.67794959_67794961delinsCTT	GRCh37
NC_000018.8:g.65945939_65945941delinsCTT	NCBI36
NG_033104.1:g.83002_83004delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255674.11:c.3160_3162delinsAAG	ENSP00000255674.7:p.Lys1054=
ENST00000638251.1:c.*1152_*1154delinsAAG	ENSP00000491968.1:n.*1152_*1154delinsAAG
ENST00000638298.1:c.149_151delinsAAG
ENST00000639128.1:n.706_708delinsAAG
ENST00000640376.1:c.2624+633_2624+635delinsAAG	ENSP00000491654.1:n.2624+633_2624+635delinsAAG
ENST00000640408.1:n.3592_3594delinsAAG
ENST00000640769.2:c.3160_3162delinsAAG MANE Select	ENSP00000491507.1:p.Lys1054=
ENST00000640931.1:c.381_383delinsAAG
ENST00000677824.1:c.783-6025_783-6023delinsAAG	ENSP00000504646.1:n.783-6025_783-6023delinsAAG
ENST00000679113.1:c.382_384delinsAAG	ENSP00000504487.1:p.Lys128=
ENST00000255674.10:c.3160_3162delinsAAG	ENSP00000255674.6:p.Lys1054=
ENST00000581161.5:c.*1474_*1476delinsAAG	ENSP00000462926.1:n.*1474_*1476delinsAAG
ENST00000583043.5:c.2441_2443delinsAAG	ENSP00000462733.1:n.2441_2443delinsAAG
NM_173630.3:c.3160_3162delinsAAG	NP_775901.3:p.Lys1054=
XM_005266679.1:c.424_426delinsAAG	XP_005266736.1:p.Lys142=
XM_006722434.2:c.3163_3165delinsAAG	XP_006722497.1:p.Lys1055=
XM_006722435.2:c.3163_3165delinsAAG	XP_006722498.1:p.Lys1055=
XM_011525902.1:c.3146+633_3146+635delinsAAG	XP_011524204.1:n.3146+633_3146+635delinsAAG
XM_011525903.1:c.2958-6025_2958-6023delinsAAG	XP_011524205.1:n.2958-6025_2958-6023delinsAAG
XM_011525904.1:c.3163_3165delinsAAG	XP_011524206.1:p.Lys1055=
XM_011525905.1:c.3163_3165delinsAAG	XP_011524207.1:p.Lys1055=
XM_011525906.1:c.1663_1665delinsAAG	XP_011524208.1:p.Lys555=
XM_011525907.1:c.3163_3165delinsAAG	XP_011524209.1:p.Lys1055=
XM_011525908.1:c.3163_3165delinsAAG	XP_011524210.1:p.Lys1055=
XR_430072.2:n.3201_3203delinsAAG
XR_935213.1:n.3201_3203delinsAAG
NM_001318520.1:c.424_426delinsAAG	NP_001305449.1:p.Lys142=
XM_006722434.3:c.3163_3165delinsAAG	XP_006722497.1:p.Lys1055=
XM_006722435.3:c.3163_3165delinsAAG	XP_006722498.1:p.Lys1055=
XM_011525902.2:c.3146+633_3146+635delinsAAG	XP_011524204.1:n.3146+633_3146+635delinsAAG
XM_011525903.2:c.2958-6025_2958-6023delinsAAG	XP_011524205.1:n.2958-6025_2958-6023delinsAAG
XM_011525904.3:c.3163_3165delinsAAG	XP_011524206.1:p.Lys1055=
XM_011525905.2:c.3163_3165delinsAAG	XP_011524207.1:p.Lys1055=
XM_011525906.2:c.1663_1665delinsAAG	XP_011524208.1:p.Lys555=
XM_011525907.2:c.3163_3165delinsAAG	XP_011524209.1:p.Lys1055=
XM_011525908.3:c.3163_3165delinsAAG	XP_011524210.1:p.Lys1055=
XM_017025693.1:c.3143+633_3143+635delinsAAG	XP_016881182.1:n.3143+633_3143+635delinsAAG
XM_017025694.1:c.2521_2523delinsAAG	XP_016881183.1:p.Lys841=
XM_017025695.1:c.2098_2100delinsAAG	XP_016881184.1:p.Lys700=
XM_017025696.1:c.1054_1056delinsAAG	XP_016881185.1:p.Lys352=
XM_024451139.1:c.2383_2385delinsAAG	XP_024306907.1:p.Lys795=
XM_024451140.1:c.2383_2385delinsAAG	XP_024306908.1:p.Lys795=
XR_430072.3:n.3231_3233delinsAAG
XR_935213.2:n.3231_3233delinsAAG
NM_001318520.2:c.424_426delinsAAG	NP_001305449.1:p.Lys142=
NM_173630.4:c.3160_3162delinsAAG MANE Select	NP_775901.3:p.Lys1054=