Canonical Allele Identifier: CA2312018558

Gene: RTTN

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.70196658_70196659delinsAG , CM000680.2:g.70196658_70196659delinsAG	GRCh38
NC_000018.9:g.67863894_67863895delinsAG , CM000680.1:g.67863894_67863895delinsAG	GRCh37
NC_000018.8:g.66014874_66014875delinsAG	NCBI36
NG_033104.1:g.14068_14069delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255674.11:c.694-11_694-10delinsCT	ENSP00000255674.7:n.694-11_694-10delinsCT
ENST00000638251.1:c.694-11_694-10delinsCT	ENSP00000491968.1:n.694-11_694-10delinsCT
ENST00000640376.1:c.175-11_175-10delinsCT	ENSP00000491654.1:n.175-11_175-10delinsCT
ENST00000640654.1:n.244-11_244-10delinsCT
ENST00000640736.1:n.542-11_542-10delinsCT
ENST00000640769.2:c.694-11_694-10delinsCT MANE Select	ENSP00000491507.1:n.694-11_694-10delinsCT
ENST00000255674.10:c.694-11_694-10delinsCT	ENSP00000255674.6:n.694-11_694-10delinsCT
ENST00000581161.5:c.694-11_694-10delinsCT	ENSP00000462926.1:n.694-11_694-10delinsCT
ENST00000581583.1:n.762-11_762-10delinsCT
ENST00000583043.5:c.64-11_64-10delinsCT	ENSP00000462733.1:n.64-11_64-10delinsCT
NM_173630.3:c.694-11_694-10delinsCT	NP_775901.3:n.694-11_694-10delinsCT
XM_005266679.1:c.-1860-11_-1860-10delinsCT	XP_005266736.1:n.-1860-11_-1860-10delinsCT
XM_006722434.2:c.694-11_694-10delinsCT	XP_006722497.1:n.694-11_694-10delinsCT
XM_006722435.2:c.694-11_694-10delinsCT	XP_006722498.1:n.694-11_694-10delinsCT
XM_011525902.1:c.694-11_694-10delinsCT	XP_011524204.1:n.694-11_694-10delinsCT
XM_011525903.1:c.694-11_694-10delinsCT	XP_011524205.1:n.694-11_694-10delinsCT
XM_011525904.1:c.694-11_694-10delinsCT	XP_011524206.1:n.694-11_694-10delinsCT
XM_011525905.1:c.694-11_694-10delinsCT	XP_011524207.1:n.694-11_694-10delinsCT
XM_011525907.1:c.694-11_694-10delinsCT	XP_011524209.1:n.694-11_694-10delinsCT
XM_011525908.1:c.694-11_694-10delinsCT	XP_011524210.1:n.694-11_694-10delinsCT
XR_430072.2:n.732-11_732-10delinsCT
XR_935213.1:n.732-11_732-10delinsCT
NM_001318520.1:c.-1860-11_-1860-10delinsCT	NP_001305449.1:n.-1860-11_-1860-10delinsCT
XM_006722434.3:c.694-11_694-10delinsCT	XP_006722497.1:n.694-11_694-10delinsCT
XM_006722435.3:c.694-11_694-10delinsCT	XP_006722498.1:n.694-11_694-10delinsCT
XM_011525902.2:c.694-11_694-10delinsCT	XP_011524204.1:n.694-11_694-10delinsCT
XM_011525903.2:c.694-11_694-10delinsCT	XP_011524205.1:n.694-11_694-10delinsCT
XM_011525904.3:c.694-11_694-10delinsCT	XP_011524206.1:n.694-11_694-10delinsCT
XM_011525905.2:c.694-11_694-10delinsCT	XP_011524207.1:n.694-11_694-10delinsCT
XM_011525907.2:c.694-11_694-10delinsCT	XP_011524209.1:n.694-11_694-10delinsCT
XM_011525908.3:c.694-11_694-10delinsCT	XP_011524210.1:n.694-11_694-10delinsCT
XM_017025693.1:c.694-11_694-10delinsCT	XP_016881182.1:n.694-11_694-10delinsCT
XM_017025694.1:c.52-11_52-10delinsCT	XP_016881183.1:n.52-11_52-10delinsCT
XM_017025696.1:c.-1478-11_-1478-10delinsCT	XP_016881185.1:n.-1478-11_-1478-10delinsCT
XM_024451139.1:c.-87-11_-87-10delinsCT	XP_024306907.1:n.-87-11_-87-10delinsCT
XM_024451140.1:c.-87-11_-87-10delinsCT	XP_024306908.1:n.-87-11_-87-10delinsCT
XR_430072.3:n.762-11_762-10delinsCT
XR_935213.2:n.762-11_762-10delinsCT
NM_001318520.2:c.-1860-11_-1860-10delinsCT	NP_001305449.1:n.-1860-11_-1860-10delinsCT
NM_173630.4:c.694-11_694-10delinsCT MANE Select	NP_775901.3:n.694-11_694-10delinsCT