Canonical Allele Identifier: CA2311988325

Gene: RTTN

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.70127974_70127979delinsTAAGAC , CM000680.2:g.70127974_70127979delinsTAAGAC	GRCh38
NC_000018.9:g.67795210_67795215delinsTAAGAC , CM000680.1:g.67795210_67795215delinsTAAGAC	GRCh37
NC_000018.8:g.65946190_65946195delinsTAAGAC	NCBI36
NG_033104.1:g.82748_82753delinsGTCTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255674.11:c.3144-238_3144-233delinsGTCTTA	ENSP00000255674.7:n.3144-238_3144-233delinsGTCTTA
ENST00000638251.1:c.*1136-238_*1136-233delinsGTCTTA	ENSP00000491968.1:n.*1136-238_*1136-233delinsGTCTTA
ENST00000638298.1:c.132+75_132+80delinsGTCTTA
ENST00000639128.1:n.690-238_690-233delinsGTCTTA
ENST00000640376.1:c.2624+379_2624+384delinsGTCTTA	ENSP00000491654.1:n.2624+379_2624+384delinsGTCTTA
ENST00000640408.1:n.3576-238_3576-233delinsGTCTTA
ENST00000640769.2:c.3144-238_3144-233delinsGTCTTA MANE Select	ENSP00000491507.1:n.3144-238_3144-233delinsGTCTTA
ENST00000640931.1:c.365-238_365-233delinsGTCTTA
ENST00000677824.1:c.783-6279_783-6274delinsGTCTTA	ENSP00000504646.1:n.783-6279_783-6274delinsGTCTTA
ENST00000679113.1:c.366-238_366-233delinsGTCTTA	ENSP00000504487.1:n.366-238_366-233delinsGTCTTA
ENST00000255674.10:c.3144-238_3144-233delinsGTCTTA	ENSP00000255674.6:n.3144-238_3144-233delinsGTCTTA
ENST00000581161.5:c.*1458-238_*1458-233delinsGTCTTA	ENSP00000462926.1:n.*1458-238_*1458-233delinsGTCTTA
ENST00000583043.5:c.2425-238_2425-233delinsGTCTTA	ENSP00000462733.1:n.2425-238_2425-233delinsGTCTTA
NM_173630.3:c.3144-238_3144-233delinsGTCTTA	NP_775901.3:n.3144-238_3144-233delinsGTCTTA
XM_005266679.1:c.408-238_408-233delinsGTCTTA	XP_005266736.1:n.408-238_408-233delinsGTCTTA
XM_006722434.2:c.3147-238_3147-233delinsGTCTTA	XP_006722497.1:n.3147-238_3147-233delinsGTCTTA
XM_006722435.2:c.3147-238_3147-233delinsGTCTTA	XP_006722498.1:n.3147-238_3147-233delinsGTCTTA
XM_011525902.1:c.3146+379_3146+384delinsGTCTTA	XP_011524204.1:n.3146+379_3146+384delinsGTCTTA
XM_011525903.1:c.2958-6279_2958-6274delinsGTCTTA	XP_011524205.1:n.2958-6279_2958-6274delinsGTCTTA
XM_011525904.1:c.3147-238_3147-233delinsGTCTTA	XP_011524206.1:n.3147-238_3147-233delinsGTCTTA
XM_011525905.1:c.3147-238_3147-233delinsGTCTTA	XP_011524207.1:n.3147-238_3147-233delinsGTCTTA
XM_011525906.1:c.1647-238_1647-233delinsGTCTTA	XP_011524208.1:n.1647-238_1647-233delinsGTCTTA
XM_011525907.1:c.3147-238_3147-233delinsGTCTTA	XP_011524209.1:n.3147-238_3147-233delinsGTCTTA
XM_011525908.1:c.3147-238_3147-233delinsGTCTTA	XP_011524210.1:n.3147-238_3147-233delinsGTCTTA
XR_430072.2:n.3185-238_3185-233delinsGTCTTA
XR_935213.1:n.3185-238_3185-233delinsGTCTTA
NM_001318520.1:c.408-238_408-233delinsGTCTTA	NP_001305449.1:n.408-238_408-233delinsGTCTTA
XM_006722434.3:c.3147-238_3147-233delinsGTCTTA	XP_006722497.1:n.3147-238_3147-233delinsGTCTTA
XM_006722435.3:c.3147-238_3147-233delinsGTCTTA	XP_006722498.1:n.3147-238_3147-233delinsGTCTTA
XM_011525902.2:c.3146+379_3146+384delinsGTCTTA	XP_011524204.1:n.3146+379_3146+384delinsGTCTTA
XM_011525903.2:c.2958-6279_2958-6274delinsGTCTTA	XP_011524205.1:n.2958-6279_2958-6274delinsGTCTTA
XM_011525904.3:c.3147-238_3147-233delinsGTCTTA	XP_011524206.1:n.3147-238_3147-233delinsGTCTTA
XM_011525905.2:c.3147-238_3147-233delinsGTCTTA	XP_011524207.1:n.3147-238_3147-233delinsGTCTTA
XM_011525906.2:c.1647-238_1647-233delinsGTCTTA	XP_011524208.1:n.1647-238_1647-233delinsGTCTTA
XM_011525907.2:c.3147-238_3147-233delinsGTCTTA	XP_011524209.1:n.3147-238_3147-233delinsGTCTTA
XM_011525908.3:c.3147-238_3147-233delinsGTCTTA	XP_011524210.1:n.3147-238_3147-233delinsGTCTTA
XM_017025693.1:c.3143+379_3143+384delinsGTCTTA	XP_016881182.1:n.3143+379_3143+384delinsGTCTTA
XM_017025694.1:c.2505-238_2505-233delinsGTCTTA	XP_016881183.1:n.2505-238_2505-233delinsGTCTTA
XM_017025695.1:c.2082-238_2082-233delinsGTCTTA	XP_016881184.1:n.2082-238_2082-233delinsGTCTTA
XM_017025696.1:c.1038-238_1038-233delinsGTCTTA	XP_016881185.1:n.1038-238_1038-233delinsGTCTTA
XM_024451139.1:c.2367-238_2367-233delinsGTCTTA	XP_024306907.1:n.2367-238_2367-233delinsGTCTTA
XM_024451140.1:c.2367-238_2367-233delinsGTCTTA	XP_024306908.1:n.2367-238_2367-233delinsGTCTTA
XR_430072.3:n.3215-238_3215-233delinsGTCTTA
XR_935213.2:n.3215-238_3215-233delinsGTCTTA
NM_001318520.2:c.408-238_408-233delinsGTCTTA	NP_001305449.1:n.408-238_408-233delinsGTCTTA
NM_173630.4:c.3144-238_3144-233delinsGTCTTA MANE Select	NP_775901.3:n.3144-238_3144-233delinsGTCTTA