Canonical Allele Identifier: CA402694149

Gene: RTTN

Linked Data

• gnomAD v4: 18-70127742-C-G
• MyVariant Identifiers: chr18:g.67794978C>G (hg19) ; chr18:g.70127742C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.70127742C>G , CM000680.2:g.70127742C>G	GRCh38
NC_000018.9:g.67794978C>G , CM000680.1:g.67794978C>G	GRCh37
NC_000018.8:g.65945958C>G	NCBI36
NG_033104.1:g.82985G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255674.11:c.3144-1G>C	ENSP00000255674.7:n.3144-1G>C
ENST00000638251.1:c.*1136-1G>C	ENSP00000491968.1:n.*1136-1G>C
ENST00000638298.1:c.133-1G>C
ENST00000639128.1:n.690-1G>C
ENST00000640376.1:c.2624+616G>C	ENSP00000491654.1:n.2624+616G>C
ENST00000640408.1:n.3576-1G>C
ENST00000640769.2:c.3144-1G>C MANE Select	ENSP00000491507.1:n.3144-1G>C
ENST00000640931.1:c.365-1G>C
ENST00000677824.1:c.783-6042G>C	ENSP00000504646.1:n.783-6042G>C
ENST00000679113.1:c.366-1G>C	ENSP00000504487.1:n.366-1G>C
ENST00000255674.10:c.3144-1G>C	ENSP00000255674.6:n.3144-1G>C
ENST00000581161.5:c.*1458-1G>C	ENSP00000462926.1:n.*1458-1G>C
ENST00000583043.5:c.2425-1G>C	ENSP00000462733.1:n.2425-1G>C
NM_173630.3:c.3144-1G>C	NP_775901.3:n.3144-1G>C
XM_005266679.1:c.408-1G>C	XP_005266736.1:n.408-1G>C
XM_006722434.2:c.3147-1G>C	XP_006722497.1:n.3147-1G>C
XM_006722435.2:c.3147-1G>C	XP_006722498.1:n.3147-1G>C
XM_011525902.1:c.3146+616G>C	XP_011524204.1:n.3146+616G>C
XM_011525903.1:c.2958-6042G>C	XP_011524205.1:n.2958-6042G>C
XM_011525904.1:c.3147-1G>C	XP_011524206.1:n.3147-1G>C
XM_011525905.1:c.3147-1G>C	XP_011524207.1:n.3147-1G>C
XM_011525906.1:c.1647-1G>C	XP_011524208.1:n.1647-1G>C
XM_011525907.1:c.3147-1G>C	XP_011524209.1:n.3147-1G>C
XM_011525908.1:c.3147-1G>C	XP_011524210.1:n.3147-1G>C
XR_430072.2:n.3185-1G>C
XR_935213.1:n.3185-1G>C
NM_001318520.1:c.408-1G>C	NP_001305449.1:n.408-1G>C
XM_006722434.3:c.3147-1G>C	XP_006722497.1:n.3147-1G>C
XM_006722435.3:c.3147-1G>C	XP_006722498.1:n.3147-1G>C
XM_011525902.2:c.3146+616G>C	XP_011524204.1:n.3146+616G>C
XM_011525903.2:c.2958-6042G>C	XP_011524205.1:n.2958-6042G>C
XM_011525904.3:c.3147-1G>C	XP_011524206.1:n.3147-1G>C
XM_011525905.2:c.3147-1G>C	XP_011524207.1:n.3147-1G>C
XM_011525906.2:c.1647-1G>C	XP_011524208.1:n.1647-1G>C
XM_011525907.2:c.3147-1G>C	XP_011524209.1:n.3147-1G>C
XM_011525908.3:c.3147-1G>C	XP_011524210.1:n.3147-1G>C
XM_017025693.1:c.3143+616G>C	XP_016881182.1:n.3143+616G>C
XM_017025694.1:c.2505-1G>C	XP_016881183.1:n.2505-1G>C
XM_017025695.1:c.2082-1G>C	XP_016881184.1:n.2082-1G>C
XM_017025696.1:c.1038-1G>C	XP_016881185.1:n.1038-1G>C
XM_024451139.1:c.2367-1G>C	XP_024306907.1:n.2367-1G>C
XM_024451140.1:c.2367-1G>C	XP_024306908.1:n.2367-1G>C
XR_430072.3:n.3215-1G>C
XR_935213.2:n.3215-1G>C
NM_001318520.2:c.408-1G>C	NP_001305449.1:n.408-1G>C
NM_173630.4:c.3144-1G>C MANE Select	NP_775901.3:n.3144-1G>C