Canonical Allele Identifier: CA2642180251

Gene: RTTN

Linked Data

• gnomAD v4: 18-70128025-CTAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.70128027_70128029del , CM000680.2:g.70128027_70128029del	GRCh38
NC_000018.9:g.67795263_67795265del , CM000680.1:g.67795263_67795265del	GRCh37
NC_000018.8:g.65946243_65946245del	NCBI36
NG_033104.1:g.82699_82701del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255674.11:c.3144-287_3144-285del	ENSP00000255674.7:n.3144-287_3144-285del
ENST00000638251.1:c.*1136-287_*1136-285del	ENSP00000491968.1:n.*1136-287_*1136-285del
ENST00000638298.1:c.132+26_132+28del
ENST00000639128.1:n.690-287_690-285del
ENST00000640376.1:c.2624+330_2624+332del	ENSP00000491654.1:n.2624+330_2624+332del
ENST00000640408.1:n.3576-287_3576-285del
ENST00000640769.2:c.3144-287_3144-285del MANE Select	ENSP00000491507.1:n.3144-287_3144-285del
ENST00000640931.1:c.365-287_365-285del
ENST00000677824.1:c.783-6328_783-6326del	ENSP00000504646.1:n.783-6328_783-6326del
ENST00000679113.1:c.366-287_366-285del	ENSP00000504487.1:n.366-287_366-285del
ENST00000255674.10:c.3144-287_3144-285del	ENSP00000255674.6:n.3144-287_3144-285del
ENST00000581161.5:c.*1458-287_*1458-285del	ENSP00000462926.1:n.*1458-287_*1458-285del
ENST00000583043.5:c.2425-287_2425-285del	ENSP00000462733.1:n.2425-287_2425-285del
NM_173630.3:c.3144-287_3144-285del	NP_775901.3:n.3144-287_3144-285del
XM_005266679.1:c.408-287_408-285del	XP_005266736.1:n.408-287_408-285del
XM_006722434.2:c.3147-287_3147-285del	XP_006722497.1:n.3147-287_3147-285del
XM_006722435.2:c.3147-287_3147-285del	XP_006722498.1:n.3147-287_3147-285del
XM_011525902.1:c.3146+330_3146+332del	XP_011524204.1:n.3146+330_3146+332del
XM_011525903.1:c.2958-6328_2958-6326del	XP_011524205.1:n.2958-6328_2958-6326del
XM_011525904.1:c.3147-287_3147-285del	XP_011524206.1:n.3147-287_3147-285del
XM_011525905.1:c.3147-287_3147-285del	XP_011524207.1:n.3147-287_3147-285del
XM_011525906.1:c.1647-287_1647-285del	XP_011524208.1:n.1647-287_1647-285del
XM_011525907.1:c.3147-287_3147-285del	XP_011524209.1:n.3147-287_3147-285del
XM_011525908.1:c.3147-287_3147-285del	XP_011524210.1:n.3147-287_3147-285del
XR_430072.2:n.3185-287_3185-285del
XR_935213.1:n.3185-287_3185-285del
NM_001318520.1:c.408-287_408-285del	NP_001305449.1:n.408-287_408-285del
XM_006722434.3:c.3147-287_3147-285del	XP_006722497.1:n.3147-287_3147-285del
XM_006722435.3:c.3147-287_3147-285del	XP_006722498.1:n.3147-287_3147-285del
XM_011525902.2:c.3146+330_3146+332del	XP_011524204.1:n.3146+330_3146+332del
XM_011525903.2:c.2958-6328_2958-6326del	XP_011524205.1:n.2958-6328_2958-6326del
XM_011525904.3:c.3147-287_3147-285del	XP_011524206.1:n.3147-287_3147-285del
XM_011525905.2:c.3147-287_3147-285del	XP_011524207.1:n.3147-287_3147-285del
XM_011525906.2:c.1647-287_1647-285del	XP_011524208.1:n.1647-287_1647-285del
XM_011525907.2:c.3147-287_3147-285del	XP_011524209.1:n.3147-287_3147-285del
XM_011525908.3:c.3147-287_3147-285del	XP_011524210.1:n.3147-287_3147-285del
XM_017025693.1:c.3143+330_3143+332del	XP_016881182.1:n.3143+330_3143+332del
XM_017025694.1:c.2505-287_2505-285del	XP_016881183.1:n.2505-287_2505-285del
XM_017025695.1:c.2082-287_2082-285del	XP_016881184.1:n.2082-287_2082-285del
XM_017025696.1:c.1038-287_1038-285del	XP_016881185.1:n.1038-287_1038-285del
XM_024451139.1:c.2367-287_2367-285del	XP_024306907.1:n.2367-287_2367-285del
XM_024451140.1:c.2367-287_2367-285del	XP_024306908.1:n.2367-287_2367-285del
XR_430072.3:n.3215-287_3215-285del
XR_935213.2:n.3215-287_3215-285del
NM_001318520.2:c.408-287_408-285del	NP_001305449.1:n.408-287_408-285del
NM_173630.4:c.3144-287_3144-285del MANE Select	NP_775901.3:n.3144-287_3144-285del