Canonical Allele Identifier: CA2642182862

Gene: RTTN

Linked Data

• gnomAD v4: 18-70196658-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.70196659dup , CM000680.2:g.70196659dup	GRCh38
NC_000018.9:g.67863895dup , CM000680.1:g.67863895dup	GRCh37
NC_000018.8:g.66014875dup	NCBI36
NG_033104.1:g.14068dup

Transcript Alleles

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