Canonical Allele Identifier: CA402694535

Gene: RTTN

Linked Data

• MyVariant Identifiers: chr18:g.67727150T>G (hg19) ; chr18:g.70059914T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.70059914T>G , CM000680.2:g.70059914T>G	GRCh38
NC_000018.9:g.67727150T>G , CM000680.1:g.67727150T>G	GRCh37
NC_000018.8:g.65878130T>G	NCBI36
NG_033104.1:g.150813A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000255674.11:c.4876A>C	ENSP00000255674.7:p.Thr1626Pro
ENST00000579986.6:c.963A>C	ENSP00000491518.1:p.Ter321Cys
ENST00000639128.1:n.2422A>C
ENST00000639487.1:c.30A>C
ENST00000640769.2:c.4876A>C MANE Select	ENSP00000491507.1:p.Thr1626Pro
ENST00000677824.1:c.2275A>C	ENSP00000504646.1:p.Thr759Pro
ENST00000679113.1:c.2228A>C	ENSP00000504487.1:n.2228A>C
ENST00000255674.10:c.4876A>C	ENSP00000255674.6:p.Thr1626Pro
ENST00000581161.5:c.*3190A>C	ENSP00000462926.1:n.*3190A>C
ENST00000583043.5:c.4157A>C	ENSP00000462733.1:n.4157A>C
NM_173630.3:c.4876A>C	NP_775901.3:p.Thr1626Pro
XM_005266679.1:c.2140A>C	XP_005266736.1:p.Thr714Pro
XM_006722434.2:c.4879A>C	XP_006722497.1:p.Thr1627Pro
XM_006722435.2:c.4879A>C	XP_006722498.1:p.Thr1627Pro
XM_011525902.1:c.4639A>C	XP_011524204.1:p.Thr1547Pro
XM_011525903.1:c.4450A>C	XP_011524205.1:p.Thr1484Pro
XM_011525904.1:c.4879A>C	XP_011524206.1:p.Thr1627Pro
XM_011525905.1:c.4879A>C	XP_011524207.1:p.Thr1627Pro
XM_011525906.1:c.3379A>C	XP_011524208.1:p.Thr1127Pro
XR_430072.2:n.4917A>C
NM_001318520.1:c.2140A>C	NP_001305449.1:p.Thr714Pro
XM_006722434.3:c.4879A>C	XP_006722497.1:p.Thr1627Pro
XM_006722435.3:c.4879A>C	XP_006722498.1:p.Thr1627Pro
XM_011525902.2:c.4639A>C	XP_011524204.1:p.Thr1547Pro
XM_011525903.2:c.4450A>C	XP_011524205.1:p.Thr1484Pro
XM_011525904.3:c.4879A>C	XP_011524206.1:p.Thr1627Pro
XM_011525905.2:c.4879A>C	XP_011524207.1:p.Thr1627Pro
XM_011525906.2:c.3379A>C	XP_011524208.1:p.Thr1127Pro
XM_017025693.1:c.4636A>C	XP_016881182.1:p.Thr1546Pro
XM_017025694.1:c.4237A>C	XP_016881183.1:p.Thr1413Pro
XM_017025695.1:c.3814A>C	XP_016881184.1:p.Thr1272Pro
XM_017025696.1:c.2770A>C	XP_016881185.1:p.Thr924Pro
XM_024451139.1:c.4099A>C	XP_024306907.1:p.Thr1367Pro
XM_024451140.1:c.4099A>C	XP_024306908.1:p.Thr1367Pro
XR_430072.3:n.4947A>C
NM_001318520.2:c.2140A>C	NP_001305449.1:p.Thr714Pro
NM_173630.4:c.4876A>C MANE Select	NP_775901.3:p.Thr1626Pro