Canonical Allele Identifier: CA402694489

Gene: RTTN

Linked Data

• MyVariant Identifiers: chr18:g.67727141G>T (hg19) ; chr18:g.70059905G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.70059905G>T , CM000680.2:g.70059905G>T	GRCh38
NC_000018.9:g.67727141G>T , CM000680.1:g.67727141G>T	GRCh37
NC_000018.8:g.65878121G>T	NCBI36
NG_033104.1:g.150822C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255674.11:c.4885C>A	ENSP00000255674.7:p.Pro1629Thr
ENST00000579986.6:c.972C>A	ENSP00000491518.1:n.972C>A
ENST00000639128.1:n.2431C>A
ENST00000639487.1:c.39C>A
ENST00000640769.2:c.4885C>A MANE Select	ENSP00000491507.1:p.Pro1629Thr
ENST00000677824.1:c.2284C>A	ENSP00000504646.1:p.Pro762Thr
ENST00000679113.1:c.2237C>A	ENSP00000504487.1:n.2237C>A
ENST00000255674.10:c.4885C>A	ENSP00000255674.6:p.Pro1629Thr
ENST00000581161.5:c.*3199C>A	ENSP00000462926.1:n.*3199C>A
ENST00000583043.5:c.4166C>A	ENSP00000462733.1:n.4166C>A
NM_173630.3:c.4885C>A	NP_775901.3:p.Pro1629Thr
XM_005266679.1:c.2149C>A	XP_005266736.1:p.Pro717Thr
XM_006722434.2:c.4888C>A	XP_006722497.1:p.Pro1630Thr
XM_006722435.2:c.4888C>A	XP_006722498.1:p.Pro1630Thr
XM_011525902.1:c.4648C>A	XP_011524204.1:p.Pro1550Thr
XM_011525903.1:c.4459C>A	XP_011524205.1:p.Pro1487Thr
XM_011525904.1:c.4888C>A	XP_011524206.1:p.Pro1630Thr
XM_011525905.1:c.4888C>A	XP_011524207.1:p.Pro1630Thr
XM_011525906.1:c.3388C>A	XP_011524208.1:p.Pro1130Thr
XR_430072.2:n.4926C>A
NM_001318520.1:c.2149C>A	NP_001305449.1:p.Pro717Thr
XM_006722434.3:c.4888C>A	XP_006722497.1:p.Pro1630Thr
XM_006722435.3:c.4888C>A	XP_006722498.1:p.Pro1630Thr
XM_011525902.2:c.4648C>A	XP_011524204.1:p.Pro1550Thr
XM_011525903.2:c.4459C>A	XP_011524205.1:p.Pro1487Thr
XM_011525904.3:c.4888C>A	XP_011524206.1:p.Pro1630Thr
XM_011525905.2:c.4888C>A	XP_011524207.1:p.Pro1630Thr
XM_011525906.2:c.3388C>A	XP_011524208.1:p.Pro1130Thr
XM_017025693.1:c.4645C>A	XP_016881182.1:p.Pro1549Thr
XM_017025694.1:c.4246C>A	XP_016881183.1:p.Pro1416Thr
XM_017025695.1:c.3823C>A	XP_016881184.1:p.Pro1275Thr
XM_017025696.1:c.2779C>A	XP_016881185.1:p.Pro927Thr
XM_024451139.1:c.4108C>A	XP_024306907.1:p.Pro1370Thr
XM_024451140.1:c.4108C>A	XP_024306908.1:p.Pro1370Thr
XR_430072.3:n.4956C>A
NM_001318520.2:c.2149C>A	NP_001305449.1:p.Pro717Thr
NM_173630.4:c.4885C>A MANE Select	NP_775901.3:p.Pro1629Thr