Canonical Allele Identifier: CA2311957243

Gene: RTTN

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.70059820C= , CM000680.2:g.70059820C=	GRCh38
NC_000018.9:g.67727056C= , CM000680.1:g.67727056C=	GRCh37
NC_000018.8:g.65878036C=	NCBI36
NG_033104.1:g.150907G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255674.11:c.4940+30G=	ENSP00000255674.7:n.4940+30G=
ENST00000579986.6:c.1027+30G=	ENSP00000491518.1:n.1027+30G=
ENST00000639128.1:n.2486+30G=
ENST00000639487.1:c.94+30G=
ENST00000640769.2:c.4940+30G= MANE Select	ENSP00000491507.1:n.4940+30G=
ENST00000677824.1:c.2339+30G=	ENSP00000504646.1:n.2339+30G=
ENST00000679113.1:c.2292+30G=	ENSP00000504487.1:n.2292+30G=
ENST00000255674.10:c.4940+30G=	ENSP00000255674.6:n.4940+30G=
ENST00000581161.5:c.*3254+30G=	ENSP00000462926.1:n.*3254+30G=
ENST00000583043.5:c.4221+30G=	ENSP00000462733.1:n.4221+30G=
NM_173630.3:c.4940+30G=	NP_775901.3:n.4940+30G=
XM_005266679.1:c.2204+30G=	XP_005266736.1:n.2204+30G=
XM_006722434.2:c.4943+30G=	XP_006722497.1:n.4943+30G=
XM_006722435.2:c.4943+30G=	XP_006722498.1:n.4943+30G=
XM_011525902.1:c.4703+30G=	XP_011524204.1:n.4703+30G=
XM_011525903.1:c.4514+30G=	XP_011524205.1:n.4514+30G=
XM_011525904.1:c.4943+30G=	XP_011524206.1:n.4943+30G=
XM_011525905.1:c.4943+30G=	XP_011524207.1:n.4943+30G=
XM_011525906.1:c.3443+30G=	XP_011524208.1:n.3443+30G=
XR_430072.2:n.4981+30G=
NM_001318520.1:c.2204+30G=	NP_001305449.1:n.2204+30G=
XM_006722434.3:c.4943+30G=	XP_006722497.1:n.4943+30G=
XM_006722435.3:c.4943+30G=	XP_006722498.1:n.4943+30G=
XM_011525902.2:c.4703+30G=	XP_011524204.1:n.4703+30G=
XM_011525903.2:c.4514+30G=	XP_011524205.1:n.4514+30G=
XM_011525904.3:c.4943+30G=	XP_011524206.1:n.4943+30G=
XM_011525905.2:c.4943+30G=	XP_011524207.1:n.4943+30G=
XM_011525906.2:c.3443+30G=	XP_011524208.1:n.3443+30G=
XM_017025693.1:c.4700+30G=	XP_016881182.1:n.4700+30G=
XM_017025694.1:c.4301+30G=	XP_016881183.1:n.4301+30G=
XM_017025695.1:c.3878+30G=	XP_016881184.1:n.3878+30G=
XM_017025696.1:c.2834+30G=	XP_016881185.1:n.2834+30G=
XM_024451139.1:c.4163+30G=	XP_024306907.1:n.4163+30G=
XM_024451140.1:c.4163+30G=	XP_024306908.1:n.4163+30G=
XR_430072.3:n.5011+30G=
NM_001318520.2:c.2204+30G=	NP_001305449.1:n.2204+30G=
NM_173630.4:c.4940+30G= MANE Select	NP_775901.3:n.4940+30G=