Canonical Allele Identifier: CA2576525125

Gene: RTTN

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.70127781_70127782insTTT , CM000680.2:g.70127781_70127782insTTT	GRCh38
NC_000018.9:g.67795017_67795018insTTT , CM000680.1:g.67795017_67795018insTTT	GRCh37
NC_000018.8:g.65945997_65945998insTTT	NCBI36
NG_033104.1:g.82946_82947insAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255674.11:c.3144-40_3144-39insAAA	ENSP00000255674.7:n.3144-40_3144-39insAAA
ENST00000638251.1:c.*1136-40_*1136-39insAAA	ENSP00000491968.1:n.*1136-40_*1136-39insAAA
ENST00000638298.1:c.133-40_133-39insAAA
ENST00000639128.1:n.690-40_690-39insAAA
ENST00000640376.1:c.2624+577_2624+578insAAA	ENSP00000491654.1:n.2624+577_2624+578insAAA
ENST00000640408.1:n.3576-40_3576-39insAAA
ENST00000640769.2:c.3144-40_3144-39insAAA MANE Select	ENSP00000491507.1:n.3144-40_3144-39insAAA
ENST00000640931.1:c.365-40_365-39insAAA
ENST00000677824.1:c.783-6081_783-6080insAAA	ENSP00000504646.1:n.783-6081_783-6080insAAA
ENST00000679113.1:c.366-40_366-39insAAA	ENSP00000504487.1:n.366-40_366-39insAAA
ENST00000255674.10:c.3144-40_3144-39insAAA	ENSP00000255674.6:n.3144-40_3144-39insAAA
ENST00000581161.5:c.*1458-40_*1458-39insAAA	ENSP00000462926.1:n.*1458-40_*1458-39insAAA
ENST00000583043.5:c.2425-40_2425-39insAAA	ENSP00000462733.1:n.2425-40_2425-39insAAA
NM_173630.3:c.3144-40_3144-39insAAA	NP_775901.3:n.3144-40_3144-39insAAA
XM_005266679.1:c.408-40_408-39insAAA	XP_005266736.1:n.408-40_408-39insAAA
XM_006722434.2:c.3147-40_3147-39insAAA	XP_006722497.1:n.3147-40_3147-39insAAA
XM_006722435.2:c.3147-40_3147-39insAAA	XP_006722498.1:n.3147-40_3147-39insAAA
XM_011525902.1:c.3146+577_3146+578insAAA	XP_011524204.1:n.3146+577_3146+578insAAA
XM_011525903.1:c.2958-6081_2958-6080insAAA	XP_011524205.1:n.2958-6081_2958-6080insAAA
XM_011525904.1:c.3147-40_3147-39insAAA	XP_011524206.1:n.3147-40_3147-39insAAA
XM_011525905.1:c.3147-40_3147-39insAAA	XP_011524207.1:n.3147-40_3147-39insAAA
XM_011525906.1:c.1647-40_1647-39insAAA	XP_011524208.1:n.1647-40_1647-39insAAA
XM_011525907.1:c.3147-40_3147-39insAAA	XP_011524209.1:n.3147-40_3147-39insAAA
XM_011525908.1:c.3147-40_3147-39insAAA	XP_011524210.1:n.3147-40_3147-39insAAA
XR_430072.2:n.3185-40_3185-39insAAA
XR_935213.1:n.3185-40_3185-39insAAA
NM_001318520.1:c.408-40_408-39insAAA	NP_001305449.1:n.408-40_408-39insAAA
XM_006722434.3:c.3147-40_3147-39insAAA	XP_006722497.1:n.3147-40_3147-39insAAA
XM_006722435.3:c.3147-40_3147-39insAAA	XP_006722498.1:n.3147-40_3147-39insAAA
XM_011525902.2:c.3146+577_3146+578insAAA	XP_011524204.1:n.3146+577_3146+578insAAA
XM_011525903.2:c.2958-6081_2958-6080insAAA	XP_011524205.1:n.2958-6081_2958-6080insAAA
XM_011525904.3:c.3147-40_3147-39insAAA	XP_011524206.1:n.3147-40_3147-39insAAA
XM_011525905.2:c.3147-40_3147-39insAAA	XP_011524207.1:n.3147-40_3147-39insAAA
XM_011525906.2:c.1647-40_1647-39insAAA	XP_011524208.1:n.1647-40_1647-39insAAA
XM_011525907.2:c.3147-40_3147-39insAAA	XP_011524209.1:n.3147-40_3147-39insAAA
XM_011525908.3:c.3147-40_3147-39insAAA	XP_011524210.1:n.3147-40_3147-39insAAA
XM_017025693.1:c.3143+577_3143+578insAAA	XP_016881182.1:n.3143+577_3143+578insAAA
XM_017025694.1:c.2505-40_2505-39insAAA	XP_016881183.1:n.2505-40_2505-39insAAA
XM_017025695.1:c.2082-40_2082-39insAAA	XP_016881184.1:n.2082-40_2082-39insAAA
XM_017025696.1:c.1038-40_1038-39insAAA	XP_016881185.1:n.1038-40_1038-39insAAA
XM_024451139.1:c.2367-40_2367-39insAAA	XP_024306907.1:n.2367-40_2367-39insAAA
XM_024451140.1:c.2367-40_2367-39insAAA	XP_024306908.1:n.2367-40_2367-39insAAA
XR_430072.3:n.3215-40_3215-39insAAA
XR_935213.2:n.3215-40_3215-39insAAA
NM_001318520.2:c.408-40_408-39insAAA	NP_001305449.1:n.408-40_408-39insAAA
NM_173630.4:c.3144-40_3144-39insAAA MANE Select	NP_775901.3:n.3144-40_3144-39insAAA