Canonical Allele Identifier: CA2311988257

Gene: RTTN

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.70127801_70127803delinsCTT , CM000680.2:g.70127801_70127803delinsCTT	GRCh38
NC_000018.9:g.67795037_67795039delinsCTT , CM000680.1:g.67795037_67795039delinsCTT	GRCh37
NC_000018.8:g.65946017_65946019delinsCTT	NCBI36
NG_033104.1:g.82924_82926delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255674.11:c.3144-62_3144-60delinsAAG	ENSP00000255674.7:n.3144-62_3144-60delinsAAG
ENST00000638251.1:c.*1136-62_*1136-60delinsAAG	ENSP00000491968.1:n.*1136-62_*1136-60delinsAAG
ENST00000638298.1:c.133-62_133-60delinsAAG
ENST00000639128.1:n.690-62_690-60delinsAAG
ENST00000640376.1:c.2624+555_2624+557delinsAAG	ENSP00000491654.1:n.2624+555_2624+557delinsAAG
ENST00000640408.1:n.3576-62_3576-60delinsAAG
ENST00000640769.2:c.3144-62_3144-60delinsAAG MANE Select	ENSP00000491507.1:n.3144-62_3144-60delinsAAG
ENST00000640931.1:c.365-62_365-60delinsAAG
ENST00000677824.1:c.783-6103_783-6101delinsAAG	ENSP00000504646.1:n.783-6103_783-6101delinsAAG
ENST00000679113.1:c.366-62_366-60delinsAAG	ENSP00000504487.1:n.366-62_366-60delinsAAG
ENST00000255674.10:c.3144-62_3144-60delinsAAG	ENSP00000255674.6:n.3144-62_3144-60delinsAAG
ENST00000581161.5:c.*1458-62_*1458-60delinsAAG	ENSP00000462926.1:n.*1458-62_*1458-60delinsAAG
ENST00000583043.5:c.2425-62_2425-60delinsAAG	ENSP00000462733.1:n.2425-62_2425-60delinsAAG
NM_173630.3:c.3144-62_3144-60delinsAAG	NP_775901.3:n.3144-62_3144-60delinsAAG
XM_005266679.1:c.408-62_408-60delinsAAG	XP_005266736.1:n.408-62_408-60delinsAAG
XM_006722434.2:c.3147-62_3147-60delinsAAG	XP_006722497.1:n.3147-62_3147-60delinsAAG
XM_006722435.2:c.3147-62_3147-60delinsAAG	XP_006722498.1:n.3147-62_3147-60delinsAAG
XM_011525902.1:c.3146+555_3146+557delinsAAG	XP_011524204.1:n.3146+555_3146+557delinsAAG
XM_011525903.1:c.2958-6103_2958-6101delinsAAG	XP_011524205.1:n.2958-6103_2958-6101delinsAAG
XM_011525904.1:c.3147-62_3147-60delinsAAG	XP_011524206.1:n.3147-62_3147-60delinsAAG
XM_011525905.1:c.3147-62_3147-60delinsAAG	XP_011524207.1:n.3147-62_3147-60delinsAAG
XM_011525906.1:c.1647-62_1647-60delinsAAG	XP_011524208.1:n.1647-62_1647-60delinsAAG
XM_011525907.1:c.3147-62_3147-60delinsAAG	XP_011524209.1:n.3147-62_3147-60delinsAAG
XM_011525908.1:c.3147-62_3147-60delinsAAG	XP_011524210.1:n.3147-62_3147-60delinsAAG
XR_430072.2:n.3185-62_3185-60delinsAAG
XR_935213.1:n.3185-62_3185-60delinsAAG
NM_001318520.1:c.408-62_408-60delinsAAG	NP_001305449.1:n.408-62_408-60delinsAAG
XM_006722434.3:c.3147-62_3147-60delinsAAG	XP_006722497.1:n.3147-62_3147-60delinsAAG
XM_006722435.3:c.3147-62_3147-60delinsAAG	XP_006722498.1:n.3147-62_3147-60delinsAAG
XM_011525902.2:c.3146+555_3146+557delinsAAG	XP_011524204.1:n.3146+555_3146+557delinsAAG
XM_011525903.2:c.2958-6103_2958-6101delinsAAG	XP_011524205.1:n.2958-6103_2958-6101delinsAAG
XM_011525904.3:c.3147-62_3147-60delinsAAG	XP_011524206.1:n.3147-62_3147-60delinsAAG
XM_011525905.2:c.3147-62_3147-60delinsAAG	XP_011524207.1:n.3147-62_3147-60delinsAAG
XM_011525906.2:c.1647-62_1647-60delinsAAG	XP_011524208.1:n.1647-62_1647-60delinsAAG
XM_011525907.2:c.3147-62_3147-60delinsAAG	XP_011524209.1:n.3147-62_3147-60delinsAAG
XM_011525908.3:c.3147-62_3147-60delinsAAG	XP_011524210.1:n.3147-62_3147-60delinsAAG
XM_017025693.1:c.3143+555_3143+557delinsAAG	XP_016881182.1:n.3143+555_3143+557delinsAAG
XM_017025694.1:c.2505-62_2505-60delinsAAG	XP_016881183.1:n.2505-62_2505-60delinsAAG
XM_017025695.1:c.2082-62_2082-60delinsAAG	XP_016881184.1:n.2082-62_2082-60delinsAAG
XM_017025696.1:c.1038-62_1038-60delinsAAG	XP_016881185.1:n.1038-62_1038-60delinsAAG
XM_024451139.1:c.2367-62_2367-60delinsAAG	XP_024306907.1:n.2367-62_2367-60delinsAAG
XM_024451140.1:c.2367-62_2367-60delinsAAG	XP_024306908.1:n.2367-62_2367-60delinsAAG
XR_430072.3:n.3215-62_3215-60delinsAAG
XR_935213.2:n.3215-62_3215-60delinsAAG
NM_001318520.2:c.408-62_408-60delinsAAG	NP_001305449.1:n.408-62_408-60delinsAAG
NM_173630.4:c.3144-62_3144-60delinsAAG MANE Select	NP_775901.3:n.3144-62_3144-60delinsAAG