Canonical Allele Identifier: CA14752490

Gene: RIN2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.19871859G>A , CM000682.2:g.19871859G>A	GRCh38
NC_000020.10:g.19852503G>A , CM000682.1:g.19852503G>A	GRCh37
NC_000020.9:g.19800503G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255006.12:c.-36-17707G>A MANE Select	ENSP00000255006.7:n.-36-17707G>A
ENST00000432334.2:n.537-17707G>A
ENST00000616029.2:n.1208G>A
ENST00000648165.1:n.617+564G>A
XM_005260731.2:c.-36-17707G>A	XP_005260788.1:n.-36-17707G>A
XM_006723574.2:c.-37+564G>A	XP_006723637.1:n.-37+564G>A
XM_006723575.2:c.-36-17707G>A	XP_006723638.1:n.-36-17707G>A
XM_011529256.1:c.16+564G>A	XP_011527558.1:n.16+564G>A
XM_006723574.4:c.-37+564G>A	XP_006723637.1:n.-37+564G>A
XM_006723575.4:c.-36-17707G>A	XP_006723638.1:n.-36-17707G>A
XM_017027887.1:c.-34+564G>A	XP_016883376.1:n.-34+564G>A
XM_017027888.1:c.-34+564G>A	XP_016883377.1:n.-34+564G>A
XM_024451911.1:c.-37+564G>A	XP_024307679.1:n.-37+564G>A
XM_024451912.1:c.-37+564G>A	XP_024307680.1:n.-37+564G>A
XM_024451913.1:c.-36-17707G>A	XP_024307681.1:n.-36-17707G>A
NM_001378238.1:c.-581-17707G>A	NP_001365167.1:n.-581-17707G>A
NM_018993.4:c.-36-17707G>A MANE Select	NP_061866.1:n.-36-17707G>A