Canonical Allele Identifier: CA402693489

Gene: RTTN

Linked Data

• MyVariant Identifiers: chr18:g.67794836C>G (hg19) ; chr18:g.70127600C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.70127600C>G , CM000680.2:g.70127600C>G	GRCh38
NC_000018.9:g.67794836C>G , CM000680.1:g.67794836C>G	GRCh37
NC_000018.8:g.65945816C>G	NCBI36
NG_033104.1:g.83127G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255674.11:c.3285G>C	ENSP00000255674.7:p.Met1095Ile
ENST00000638251.1:c.*1277G>C	ENSP00000491968.1:n.*1277G>C
ENST00000638298.1:c.274G>C
ENST00000639128.1:n.831G>C
ENST00000640376.1:c.2624+758G>C	ENSP00000491654.1:n.2624+758G>C
ENST00000640408.1:n.3717G>C
ENST00000640769.2:c.3285G>C MANE Select	ENSP00000491507.1:p.Met1095Ile
ENST00000640931.1:c.506G>C
ENST00000677824.1:c.783-5900G>C	ENSP00000504646.1:n.783-5900G>C
ENST00000679113.1:c.507G>C	ENSP00000504487.1:p.Met169Ile
ENST00000255674.10:c.3285G>C	ENSP00000255674.6:p.Met1095Ile
ENST00000581161.5:c.*1599G>C	ENSP00000462926.1:n.*1599G>C
ENST00000583043.5:c.2566G>C	ENSP00000462733.1:n.2566G>C
NM_173630.3:c.3285G>C	NP_775901.3:p.Met1095Ile
XM_005266679.1:c.549G>C	XP_005266736.1:p.Met183Ile
XM_006722434.2:c.3288G>C	XP_006722497.1:p.Met1096Ile
XM_006722435.2:c.3288G>C	XP_006722498.1:p.Met1096Ile
XM_011525902.1:c.3146+758G>C	XP_011524204.1:n.3146+758G>C
XM_011525903.1:c.2958-5900G>C	XP_011524205.1:n.2958-5900G>C
XM_011525904.1:c.3288G>C	XP_011524206.1:p.Met1096Ile
XM_011525905.1:c.3288G>C	XP_011524207.1:p.Met1096Ile
XM_011525906.1:c.1788G>C	XP_011524208.1:p.Met596Ile
XM_011525907.1:c.3288G>C	XP_011524209.1:p.Met1096Ile
XM_011525908.1:c.3288G>C	XP_011524210.1:p.Met1096Ile
XR_430072.2:n.3326G>C
XR_935213.1:n.3326G>C
NM_001318520.1:c.549G>C	NP_001305449.1:p.Met183Ile
XM_006722434.3:c.3288G>C	XP_006722497.1:p.Met1096Ile
XM_006722435.3:c.3288G>C	XP_006722498.1:p.Met1096Ile
XM_011525902.2:c.3146+758G>C	XP_011524204.1:n.3146+758G>C
XM_011525903.2:c.2958-5900G>C	XP_011524205.1:n.2958-5900G>C
XM_011525904.3:c.3288G>C	XP_011524206.1:p.Met1096Ile
XM_011525905.2:c.3288G>C	XP_011524207.1:p.Met1096Ile
XM_011525906.2:c.1788G>C	XP_011524208.1:p.Met596Ile
XM_011525907.2:c.3288G>C	XP_011524209.1:p.Met1096Ile
XM_011525908.3:c.3288G>C	XP_011524210.1:p.Met1096Ile
XM_017025693.1:c.3143+758G>C	XP_016881182.1:n.3143+758G>C
XM_017025694.1:c.2646G>C	XP_016881183.1:p.Met882Ile
XM_017025695.1:c.2223G>C	XP_016881184.1:p.Met741Ile
XM_017025696.1:c.1179G>C	XP_016881185.1:p.Met393Ile
XM_024451139.1:c.2508G>C	XP_024306907.1:p.Met836Ile
XM_024451140.1:c.2508G>C	XP_024306908.1:p.Met836Ile
XR_430072.3:n.3356G>C
XR_935213.2:n.3356G>C
NM_001318520.2:c.549G>C	NP_001305449.1:p.Met183Ile
NM_173630.4:c.3285G>C MANE Select	NP_775901.3:p.Met1095Ile