Canonical Allele Identifier: CA709972364

Gene: RIN3

Linked Data

• dbSNP Id: rs1382028869
• MyVariant Identifiers: chr14:g.93103388T>C (hg19) ; chr14:g.92637043T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92637043T>C , CM000676.2:g.92637043T>C	GRCh38
NC_000014.8:g.93103388T>C , CM000676.1:g.93103388T>C	GRCh37
NC_000014.7:g.92173141T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000216487.12:c.441-4195T>C MANE Select	ENSP00000216487.7:n.441-4195T>C
ENST00000216487.11:c.441-4195T>C	ENSP00000216487.7:n.441-4195T>C
ENST00000418924.6:n.340-4195T>C
ENST00000554888.1:n.8-4195T>C
ENST00000555589.5:c.368-4195T>C	ENSP00000450682.1:n.368-4195T>C
ENST00000620541.4:c.441-4195T>C	ENSP00000480603.1:n.441-4195T>C
NM_024832.3:c.441-4195T>C	NP_079108.3:n.441-4195T>C
XM_011537163.1:c.216-4195T>C	XP_011535465.1:n.216-4195T>C
XM_011537164.1:c.213-4195T>C	XP_011535466.1:n.213-4195T>C
XM_011537165.1:c.-571-4195T>C	XP_011535467.1:n.-571-4195T>C
NM_001319987.1:c.216-4195T>C	NP_001306916.1:n.216-4195T>C
NM_024832.4:c.441-4195T>C	NP_079108.3:n.441-4195T>C
XM_011537164.3:c.213-4195T>C	XP_011535466.1:n.213-4195T>C
XM_011537165.3:c.-571-4195T>C	XP_011535467.1:n.-571-4195T>C
XM_017021651.2:c.348-4195T>C	XP_016877140.1:n.348-4195T>C
XM_017021652.1:c.441-4195T>C	XP_016877141.1:n.441-4195T>C
XM_017021653.1:c.441-4195T>C	XP_016877142.1:n.441-4195T>C
XM_017021654.1:c.441-4195T>C	XP_016877143.1:n.441-4195T>C
NM_024832.5:c.441-4195T>C MANE Select	NP_079108.3:n.441-4195T>C
NM_001319987.2:c.216-4195T>C	NP_001306916.1:n.216-4195T>C