Canonical Allele Identifier: CA630873133

Gene: RTTN

Linked Data

• gnomAD v2: 18-67794979-T-TAAAA
• MyVariant Identifiers: chr18:g.67794979_67794980insAAAA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.70127744_70127745insAAAA , CM000680.2:g.70127744_70127745insAAAA	GRCh38
NC_000018.9:g.67794980_67794981insAAAA , CM000680.1:g.67794980_67794981insAAAA	GRCh37
NC_000018.8:g.65945960_65945961insAAAA	NCBI36
NG_033104.1:g.82983_82984insTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255674.11:c.3144-3_3144-2insTTTT	ENSP00000255674.7:n.3144-3_3144-2insTTTT
ENST00000638251.1:c.*1136-3_*1136-2insTTTT	ENSP00000491968.1:n.*1136-3_*1136-2insTTTT
ENST00000638298.1:c.133-3_133-2insTTTT
ENST00000639128.1:n.690-3_690-2insTTTT
ENST00000640376.1:c.2624+614_2624+615insTTTT	ENSP00000491654.1:n.2624+614_2624+615insTTTT
ENST00000640408.1:n.3576-3_3576-2insTTTT
ENST00000640769.2:c.3144-3_3144-2insTTTT MANE Select	ENSP00000491507.1:n.3144-3_3144-2insTTTT
ENST00000640931.1:c.365-3_365-2insTTTT
ENST00000677824.1:c.783-6044_783-6043insTTTT	ENSP00000504646.1:n.783-6044_783-6043insTTTT
ENST00000679113.1:c.366-3_366-2insTTTT	ENSP00000504487.1:n.366-3_366-2insTTTT
ENST00000255674.10:c.3144-3_3144-2insTTTT	ENSP00000255674.6:n.3144-3_3144-2insTTTT
ENST00000581161.5:c.*1458-3_*1458-2insTTTT	ENSP00000462926.1:n.*1458-3_*1458-2insTTTT
ENST00000583043.5:c.2425-3_2425-2insTTTT	ENSP00000462733.1:n.2425-3_2425-2insTTTT
NM_173630.3:c.3144-3_3144-2insTTTT	NP_775901.3:n.3144-3_3144-2insTTTT
XM_005266679.1:c.408-3_408-2insTTTT	XP_005266736.1:n.408-3_408-2insTTTT
XM_006722434.2:c.3147-3_3147-2insTTTT	XP_006722497.1:n.3147-3_3147-2insTTTT
XM_006722435.2:c.3147-3_3147-2insTTTT	XP_006722498.1:n.3147-3_3147-2insTTTT
XM_011525902.1:c.3146+614_3146+615insTTTT	XP_011524204.1:n.3146+614_3146+615insTTTT
XM_011525903.1:c.2958-6044_2958-6043insTTTT	XP_011524205.1:n.2958-6044_2958-6043insTTTT
XM_011525904.1:c.3147-3_3147-2insTTTT	XP_011524206.1:n.3147-3_3147-2insTTTT
XM_011525905.1:c.3147-3_3147-2insTTTT	XP_011524207.1:n.3147-3_3147-2insTTTT
XM_011525906.1:c.1647-3_1647-2insTTTT	XP_011524208.1:n.1647-3_1647-2insTTTT
XM_011525907.1:c.3147-3_3147-2insTTTT	XP_011524209.1:n.3147-3_3147-2insTTTT
XM_011525908.1:c.3147-3_3147-2insTTTT	XP_011524210.1:n.3147-3_3147-2insTTTT
XR_430072.2:n.3185-3_3185-2insTTTT
XR_935213.1:n.3185-3_3185-2insTTTT
NM_001318520.1:c.408-3_408-2insTTTT	NP_001305449.1:n.408-3_408-2insTTTT
XM_006722434.3:c.3147-3_3147-2insTTTT	XP_006722497.1:n.3147-3_3147-2insTTTT
XM_006722435.3:c.3147-3_3147-2insTTTT	XP_006722498.1:n.3147-3_3147-2insTTTT
XM_011525902.2:c.3146+614_3146+615insTTTT	XP_011524204.1:n.3146+614_3146+615insTTTT
XM_011525903.2:c.2958-6044_2958-6043insTTTT	XP_011524205.1:n.2958-6044_2958-6043insTTTT
XM_011525904.3:c.3147-3_3147-2insTTTT	XP_011524206.1:n.3147-3_3147-2insTTTT
XM_011525905.2:c.3147-3_3147-2insTTTT	XP_011524207.1:n.3147-3_3147-2insTTTT
XM_011525906.2:c.1647-3_1647-2insTTTT	XP_011524208.1:n.1647-3_1647-2insTTTT
XM_011525907.2:c.3147-3_3147-2insTTTT	XP_011524209.1:n.3147-3_3147-2insTTTT
XM_011525908.3:c.3147-3_3147-2insTTTT	XP_011524210.1:n.3147-3_3147-2insTTTT
XM_017025693.1:c.3143+614_3143+615insTTTT	XP_016881182.1:n.3143+614_3143+615insTTTT
XM_017025694.1:c.2505-3_2505-2insTTTT	XP_016881183.1:n.2505-3_2505-2insTTTT
XM_017025695.1:c.2082-3_2082-2insTTTT	XP_016881184.1:n.2082-3_2082-2insTTTT
XM_017025696.1:c.1038-3_1038-2insTTTT	XP_016881185.1:n.1038-3_1038-2insTTTT
XM_024451139.1:c.2367-3_2367-2insTTTT	XP_024306907.1:n.2367-3_2367-2insTTTT
XM_024451140.1:c.2367-3_2367-2insTTTT	XP_024306908.1:n.2367-3_2367-2insTTTT
XR_430072.3:n.3215-3_3215-2insTTTT
XR_935213.2:n.3215-3_3215-2insTTTT
NM_001318520.2:c.408-3_408-2insTTTT	NP_001305449.1:n.408-3_408-2insTTTT
NM_173630.4:c.3144-3_3144-2insTTTT MANE Select	NP_775901.3:n.3144-3_3144-2insTTTT