Canonical Allele Identifier: CA2311988345

Gene: RTTN

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.70128014_70128017delinsTCAC , CM000680.2:g.70128014_70128017delinsTCAC	GRCh38
NC_000018.9:g.67795250_67795253delinsTCAC , CM000680.1:g.67795250_67795253delinsTCAC	GRCh37
NC_000018.8:g.65946230_65946233delinsTCAC	NCBI36
NG_033104.1:g.82710_82713delinsGTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255674.11:c.3144-276_3144-273delinsGTGA	ENSP00000255674.7:n.3144-276_3144-273delinsGTGA
ENST00000638251.1:c.*1136-276_*1136-273delinsGTGA	ENSP00000491968.1:n.*1136-276_*1136-273delinsGTGA
ENST00000638298.1:c.132+37_132+40delinsGTGA
ENST00000639128.1:n.690-276_690-273delinsGTGA
ENST00000640376.1:c.2624+341_2624+344delinsGTGA	ENSP00000491654.1:n.2624+341_2624+344delinsGTGA
ENST00000640408.1:n.3576-276_3576-273delinsGTGA
ENST00000640769.2:c.3144-276_3144-273delinsGTGA MANE Select	ENSP00000491507.1:n.3144-276_3144-273delinsGTGA
ENST00000640931.1:c.365-276_365-273delinsGTGA
ENST00000677824.1:c.783-6317_783-6314delinsGTGA	ENSP00000504646.1:n.783-6317_783-6314delinsGTGA
ENST00000679113.1:c.366-276_366-273delinsGTGA	ENSP00000504487.1:n.366-276_366-273delinsGTGA
ENST00000255674.10:c.3144-276_3144-273delinsGTGA	ENSP00000255674.6:n.3144-276_3144-273delinsGTGA
ENST00000581161.5:c.*1458-276_*1458-273delinsGTGA	ENSP00000462926.1:n.*1458-276_*1458-273delinsGTGA
ENST00000583043.5:c.2425-276_2425-273delinsGTGA	ENSP00000462733.1:n.2425-276_2425-273delinsGTGA
NM_173630.3:c.3144-276_3144-273delinsGTGA	NP_775901.3:n.3144-276_3144-273delinsGTGA
XM_005266679.1:c.408-276_408-273delinsGTGA	XP_005266736.1:n.408-276_408-273delinsGTGA
XM_006722434.2:c.3147-276_3147-273delinsGTGA	XP_006722497.1:n.3147-276_3147-273delinsGTGA
XM_006722435.2:c.3147-276_3147-273delinsGTGA	XP_006722498.1:n.3147-276_3147-273delinsGTGA
XM_011525902.1:c.3146+341_3146+344delinsGTGA	XP_011524204.1:n.3146+341_3146+344delinsGTGA
XM_011525903.1:c.2958-6317_2958-6314delinsGTGA	XP_011524205.1:n.2958-6317_2958-6314delinsGTGA
XM_011525904.1:c.3147-276_3147-273delinsGTGA	XP_011524206.1:n.3147-276_3147-273delinsGTGA
XM_011525905.1:c.3147-276_3147-273delinsGTGA	XP_011524207.1:n.3147-276_3147-273delinsGTGA
XM_011525906.1:c.1647-276_1647-273delinsGTGA	XP_011524208.1:n.1647-276_1647-273delinsGTGA
XM_011525907.1:c.3147-276_3147-273delinsGTGA	XP_011524209.1:n.3147-276_3147-273delinsGTGA
XM_011525908.1:c.3147-276_3147-273delinsGTGA	XP_011524210.1:n.3147-276_3147-273delinsGTGA
XR_430072.2:n.3185-276_3185-273delinsGTGA
XR_935213.1:n.3185-276_3185-273delinsGTGA
NM_001318520.1:c.408-276_408-273delinsGTGA	NP_001305449.1:n.408-276_408-273delinsGTGA
XM_006722434.3:c.3147-276_3147-273delinsGTGA	XP_006722497.1:n.3147-276_3147-273delinsGTGA
XM_006722435.3:c.3147-276_3147-273delinsGTGA	XP_006722498.1:n.3147-276_3147-273delinsGTGA
XM_011525902.2:c.3146+341_3146+344delinsGTGA	XP_011524204.1:n.3146+341_3146+344delinsGTGA
XM_011525903.2:c.2958-6317_2958-6314delinsGTGA	XP_011524205.1:n.2958-6317_2958-6314delinsGTGA
XM_011525904.3:c.3147-276_3147-273delinsGTGA	XP_011524206.1:n.3147-276_3147-273delinsGTGA
XM_011525905.2:c.3147-276_3147-273delinsGTGA	XP_011524207.1:n.3147-276_3147-273delinsGTGA
XM_011525906.2:c.1647-276_1647-273delinsGTGA	XP_011524208.1:n.1647-276_1647-273delinsGTGA
XM_011525907.2:c.3147-276_3147-273delinsGTGA	XP_011524209.1:n.3147-276_3147-273delinsGTGA
XM_011525908.3:c.3147-276_3147-273delinsGTGA	XP_011524210.1:n.3147-276_3147-273delinsGTGA
XM_017025693.1:c.3143+341_3143+344delinsGTGA	XP_016881182.1:n.3143+341_3143+344delinsGTGA
XM_017025694.1:c.2505-276_2505-273delinsGTGA	XP_016881183.1:n.2505-276_2505-273delinsGTGA
XM_017025695.1:c.2082-276_2082-273delinsGTGA	XP_016881184.1:n.2082-276_2082-273delinsGTGA
XM_017025696.1:c.1038-276_1038-273delinsGTGA	XP_016881185.1:n.1038-276_1038-273delinsGTGA
XM_024451139.1:c.2367-276_2367-273delinsGTGA	XP_024306907.1:n.2367-276_2367-273delinsGTGA
XM_024451140.1:c.2367-276_2367-273delinsGTGA	XP_024306908.1:n.2367-276_2367-273delinsGTGA
XR_430072.3:n.3215-276_3215-273delinsGTGA
XR_935213.2:n.3215-276_3215-273delinsGTGA
NM_001318520.2:c.408-276_408-273delinsGTGA	NP_001305449.1:n.408-276_408-273delinsGTGA
NM_173630.4:c.3144-276_3144-273delinsGTGA MANE Select	NP_775901.3:n.3144-276_3144-273delinsGTGA