Canonical Allele Identifier: CA3210257

Gene: RETREG1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.16475251A>G , CM000667.2:g.16475251A>G	GRCh38
NC_000005.9:g.16475360A>G , CM000667.1:g.16475360A>G	GRCh37
NC_000005.8:g.16528360A>G	NCBI36
NG_016644.2:g.146759T>C , LRG_363:g.146759T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509977.2:n.649-17T>C
ENST00000510362.6:c.476-17T>C	ENSP00000425089.2:n.476-17T>C
ENST00000682033.1:c.127-17T>C
ENST00000682142.1:c.698-17T>C	ENSP00000506804.1:n.698-17T>C
ENST00000682229.1:c.1157-17T>C	ENSP00000507342.1:n.1157-17T>C
ENST00000682564.1:c.998-17T>C	ENSP00000508099.1:n.998-17T>C
ENST00000682628.1:c.476-17T>C	ENSP00000507536.1:n.476-17T>C
ENST00000682982.1:n.1775-17T>C
ENST00000683045.1:n.5545-17T>C
ENST00000683130.1:c.*247-17T>C	ENSP00000507709.1:n.*247-17T>C
ENST00000683169.1:n.1500-17T>C
ENST00000683414.1:c.476-17T>C	ENSP00000508335.1:n.476-17T>C
ENST00000683527.1:c.*300-17T>C	ENSP00000507253.1:n.*300-17T>C
ENST00000683539.1:c.476-17T>C	ENSP00000507466.1:n.476-17T>C
ENST00000684456.1:c.-68-17T>C	ENSP00000508060.1:n.-68-17T>C
ENST00000684521.1:c.863-17T>C	ENSP00000507521.1:n.863-17T>C
ENST00000684695.1:n.3271-17T>C
ENST00000306320.10:c.1001-17T>C MANE Select	ENSP00000304642.9:n.1001-17T>C
ENST00000306320.9:c.1001-17T>C	ENSP00000304642.9:n.1001-17T>C
ENST00000399793.6:c.578-17T>C	ENSP00000382691.2:n.578-17T>C
ENST00000509977.1:n.637-17T>C
ENST00000510362.5:c.160-17T>C
NM_001034850.2:c.1001-17T>C , LRG_363t1:c.1001-17T>C	NP_001030022.1:n.1001-17T>C
NM_019000.4:c.578-17T>C	NP_061873.2:n.578-17T>C
XM_011514053.1:c.1121-17T>C	XP_011512355.1:n.1121-17T>C
XM_011514054.1:c.698-17T>C	XP_011512356.1:n.698-17T>C
XM_011514055.1:c.602-17T>C	XP_011512357.1:n.602-17T>C
XM_011514053.3:c.1121-17T>C	XP_011512355.1:n.1121-17T>C
XM_011514054.2:c.698-17T>C	XP_011512356.1:n.698-17T>C
XM_011514055.3:c.602-17T>C	XP_011512357.1:n.602-17T>C
XM_024446117.1:c.476-17T>C	XP_024301885.1:n.476-17T>C
XM_024446118.1:c.476-17T>C	XP_024301886.1:n.476-17T>C
NM_001034850.3:c.1001-17T>C MANE Select	NP_001030022.1:n.1001-17T>C
NM_019000.5:c.578-17T>C	NP_061873.2:n.578-17T>C