Canonical Allele Identifier: CA2642180167

Gene: RTTN

Linked Data

• gnomAD v4: 18-70127843-ATTTTC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.70127848_70127852del , CM000680.2:g.70127848_70127852del	GRCh38
NC_000018.9:g.67795084_67795088del , CM000680.1:g.67795084_67795088del	GRCh37
NC_000018.8:g.65946064_65946068del	NCBI36
NG_033104.1:g.82879_82883del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255674.11:c.3144-107_3144-103del	ENSP00000255674.7:n.3144-107_3144-103del
ENST00000638251.1:c.*1136-107_*1136-103del	ENSP00000491968.1:n.*1136-107_*1136-103del
ENST00000638298.1:c.133-107_133-103del
ENST00000639128.1:n.690-107_690-103del
ENST00000640376.1:c.2624+510_2624+514del	ENSP00000491654.1:n.2624+510_2624+514del
ENST00000640408.1:n.3576-107_3576-103del
ENST00000640769.2:c.3144-107_3144-103del MANE Select	ENSP00000491507.1:n.3144-107_3144-103del
ENST00000640931.1:c.365-107_365-103del
ENST00000677824.1:c.783-6148_783-6144del	ENSP00000504646.1:n.783-6148_783-6144del
ENST00000679113.1:c.366-107_366-103del	ENSP00000504487.1:n.366-107_366-103del
ENST00000255674.10:c.3144-107_3144-103del	ENSP00000255674.6:n.3144-107_3144-103del
ENST00000581161.5:c.*1458-107_*1458-103del	ENSP00000462926.1:n.*1458-107_*1458-103del
ENST00000583043.5:c.2425-107_2425-103del	ENSP00000462733.1:n.2425-107_2425-103del
NM_173630.3:c.3144-107_3144-103del	NP_775901.3:n.3144-107_3144-103del
XM_005266679.1:c.408-107_408-103del	XP_005266736.1:n.408-107_408-103del
XM_006722434.2:c.3147-107_3147-103del	XP_006722497.1:n.3147-107_3147-103del
XM_006722435.2:c.3147-107_3147-103del	XP_006722498.1:n.3147-107_3147-103del
XM_011525902.1:c.3146+510_3146+514del	XP_011524204.1:n.3146+510_3146+514del
XM_011525903.1:c.2958-6148_2958-6144del	XP_011524205.1:n.2958-6148_2958-6144del
XM_011525904.1:c.3147-107_3147-103del	XP_011524206.1:n.3147-107_3147-103del
XM_011525905.1:c.3147-107_3147-103del	XP_011524207.1:n.3147-107_3147-103del
XM_011525906.1:c.1647-107_1647-103del	XP_011524208.1:n.1647-107_1647-103del
XM_011525907.1:c.3147-107_3147-103del	XP_011524209.1:n.3147-107_3147-103del
XM_011525908.1:c.3147-107_3147-103del	XP_011524210.1:n.3147-107_3147-103del
XR_430072.2:n.3185-107_3185-103del
XR_935213.1:n.3185-107_3185-103del
NM_001318520.1:c.408-107_408-103del	NP_001305449.1:n.408-107_408-103del
XM_006722434.3:c.3147-107_3147-103del	XP_006722497.1:n.3147-107_3147-103del
XM_006722435.3:c.3147-107_3147-103del	XP_006722498.1:n.3147-107_3147-103del
XM_011525902.2:c.3146+510_3146+514del	XP_011524204.1:n.3146+510_3146+514del
XM_011525903.2:c.2958-6148_2958-6144del	XP_011524205.1:n.2958-6148_2958-6144del
XM_011525904.3:c.3147-107_3147-103del	XP_011524206.1:n.3147-107_3147-103del
XM_011525905.2:c.3147-107_3147-103del	XP_011524207.1:n.3147-107_3147-103del
XM_011525906.2:c.1647-107_1647-103del	XP_011524208.1:n.1647-107_1647-103del
XM_011525907.2:c.3147-107_3147-103del	XP_011524209.1:n.3147-107_3147-103del
XM_011525908.3:c.3147-107_3147-103del	XP_011524210.1:n.3147-107_3147-103del
XM_017025693.1:c.3143+510_3143+514del	XP_016881182.1:n.3143+510_3143+514del
XM_017025694.1:c.2505-107_2505-103del	XP_016881183.1:n.2505-107_2505-103del
XM_017025695.1:c.2082-107_2082-103del	XP_016881184.1:n.2082-107_2082-103del
XM_017025696.1:c.1038-107_1038-103del	XP_016881185.1:n.1038-107_1038-103del
XM_024451139.1:c.2367-107_2367-103del	XP_024306907.1:n.2367-107_2367-103del
XM_024451140.1:c.2367-107_2367-103del	XP_024306908.1:n.2367-107_2367-103del
XR_430072.3:n.3215-107_3215-103del
XR_935213.2:n.3215-107_3215-103del
NM_001318520.2:c.408-107_408-103del	NP_001305449.1:n.408-107_408-103del
NM_173630.4:c.3144-107_3144-103del MANE Select	NP_775901.3:n.3144-107_3144-103del