Canonical Allele Identifier: CA312907138

Gene: RIN2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.19886609del , CM000682.2:g.19886609del	GRCh38
NC_000020.10:g.19867253del , CM000682.1:g.19867253del	GRCh37
NC_000020.9:g.19815253del	NCBI36
NG_016310.1:g.2044del
NG_016310.2:g.2044del

Transcript Alleles

HGVS	Amino-acid Change
NM_018993.4:c.-36-2957del MANE Select	NP_061866.1:n.-36-2957del
ENST00000255006.12:c.-36-2957del MANE Select	ENSP00000255006.7:n.-36-2957del
NM_001242581.1:c.-61del	NP_001229510.1:n.-61del
NM_001378238.1:c.-581-2957del	NP_001365167.1:n.-581-2957del
ENST00000255006.10:c.-61del	ENSP00000255006.6:n.-61del
ENST00000432334.2:n.537-2957del
ENST00000648165.1:n.618-2957del
ENST00000648440.1:c.-208del	ENSP00000498085.1:n.-208del
XM_005260731.2:c.-36-2957del	XP_005260788.1:n.-36-2957del
XM_006723574.2:c.-36-2957del	XP_006723637.1:n.-36-2957del
XM_006723574.4:c.-36-2957del	XP_006723637.1:n.-36-2957del
XM_006723575.2:c.-36-2957del	XP_006723638.1:n.-36-2957del
XM_006723575.4:c.-36-2957del	XP_006723638.1:n.-36-2957del
XM_011529256.1:c.17-102del	XP_011527558.1:n.17-102del
XM_011529258.1:c.-37+1469del	XP_011527560.1:n.-37+1469del
XM_011529258.2:c.-37+1469del	XP_011527560.1:n.-37+1469del
XM_017027887.1:c.-33-28del	XP_016883376.1:n.-33-28del
XM_017027888.1:c.-33-28del	XP_016883377.1:n.-33-28del
XM_017027890.1:c.-106-102del	XP_016883379.1:n.-106-102del
XM_024451911.1:c.-36-2957del	XP_024307679.1:n.-36-2957del
XM_024451912.1:c.-36-2957del	XP_024307680.1:n.-36-2957del
XM_024451913.1:c.-36-2957del	XP_024307681.1:n.-36-2957del