Canonical Allele Identifier: CA2842693460
Community Standard Title: NM_001395490.1(TRERF1):c.1635+465C>T
Gene: TRERF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42264239G>A , CM000668.2:g.42264239G>A GRCh38
NC_000006.11:g.42231977G>A , CM000668.1:g.42231977G>A GRCh37
NC_000006.10:g.42339955G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001395490.1:c.1635+465C>T MANE Select NP_001382419.1:n.1635+465C>T
ENST00000695948.1:c.1635+465C>T MANE Select ENSP00000512293.1:n.1635+465C>T
NM_001297573.1:c.1635+465C>T NP_001284502.1:n.1635+465C>T
NM_001297573.2:c.1635+465C>T NP_001284502.1:n.1635+465C>T
NM_001297574.1:c.1635+465C>T NP_001284503.1:n.1635+465C>T
NM_001391983.1:c.1635+465C>T NP_001378912.1:n.1635+465C>T
NM_001391984.1:c.1635+465C>T NP_001378913.1:n.1635+465C>T
NM_033502.3:c.1635+465C>T NP_277037.1:n.1635+465C>T
NM_033502.4:c.1635+465C>T NP_277037.1:n.1635+465C>T
ENST00000340840.6:c.1635+465C>T ENSP00000339438.2:n.1635+465C>T
ENST00000354325.2:c.1635+465C>T ENSP00000346285.2:n.1635+465C>T
ENST00000372917.8:c.1152+465C>T ENSP00000362008.5:n.1152+465C>T
ENST00000372917.9:c.*1118+465C>T ENSP00000362008.6:n.*1118+465C>T
ENST00000372922.8:c.1635+465C>T ENSP00000362013.4:n.1635+465C>T
ENST00000541110.5:c.1635+465C>T ENSP00000439689.1:n.1635+465C>T
ENST00000695947.1:c.*1118+465C>T ENSP00000512280.1:n.*1118+465C>T
ENST00000695966.1:c.1635+465C>T ENSP00000512292.1:n.1635+465C>T
XM_006715145.2:c.1635+465C>T XP_006715208.1:n.1635+465C>T
XM_006715147.2:c.1635+465C>T XP_006715210.1:n.1635+465C>T
XM_006715148.2:c.1635+465C>T XP_006715211.1:n.1635+465C>T
XM_011514741.1:c.1635+465C>T XP_011513043.1:n.1635+465C>T
XM_011514741.2:c.1635+465C>T XP_011513043.1:n.1635+465C>T
XM_011514742.1:c.1635+465C>T XP_011513044.1:n.1635+465C>T
XM_011514742.2:c.1635+465C>T XP_011513044.1:n.1635+465C>T
XM_011514743.1:c.1635+465C>T XP_011513045.1:n.1635+465C>T
XM_011514743.2:c.1635+465C>T XP_011513045.1:n.1635+465C>T
XM_011514744.1:c.1635+465C>T XP_011513046.1:n.1635+465C>T
XM_011514745.1:c.1635+465C>T XP_011513047.1:n.1635+465C>T
XM_011514746.1:c.1635+465C>T XP_011513048.1:n.1635+465C>T
XM_011514747.1:c.1635+465C>T XP_011513049.1:n.1635+465C>T
XM_011514748.1:c.1635+465C>T XP_011513050.1:n.1635+465C>T
XM_011514749.1:c.1635+465C>T XP_011513051.1:n.1635+465C>T
XM_011514750.1:c.1635+465C>T XP_011513052.1:n.1635+465C>T
XM_011514751.1:c.1635+465C>T XP_011513053.1:n.1635+465C>T
XM_011514752.1:c.1635+465C>T XP_011513054.1:n.1635+465C>T
XM_017011034.1:c.1635+465C>T XP_016866523.1:n.1635+465C>T
XM_017011035.1:c.1635+465C>T XP_016866524.1:n.1635+465C>T
XM_017011036.1:c.1635+465C>T XP_016866525.1:n.1635+465C>T
XM_017011037.1:c.1635+465C>T XP_016866526.1:n.1635+465C>T
XM_017011038.1:c.1635+465C>T XP_016866527.1:n.1635+465C>T
XM_017011039.1:c.1635+465C>T XP_016866528.1:n.1635+465C>T
XM_017011040.1:c.1635+465C>T XP_016866529.1:n.1635+465C>T
XM_017011041.1:c.1635+465C>T XP_016866530.1:n.1635+465C>T
XM_017011042.1:c.1635+465C>T XP_016866531.1:n.1635+465C>T
XM_017011043.1:c.1635+465C>T XP_016866532.1:n.1635+465C>T
XM_017011044.1:c.1635+465C>T XP_016866533.1:n.1635+465C>T
XM_017011045.1:c.1635+465C>T XP_016866534.1:n.1635+465C>T
XM_017011046.1:c.1635+465C>T XP_016866535.1:n.1635+465C>T
XM_017011047.1:c.1635+465C>T XP_016866536.1:n.1635+465C>T
XM_017011048.1:c.1635+465C>T XP_016866537.1:n.1635+465C>T
XM_017011049.1:c.1635+465C>T XP_016866538.1:n.1635+465C>T
XM_017011050.1:c.1635+465C>T XP_016866539.1:n.1635+465C>T
XM_017011051.1:c.1635+465C>T XP_016866540.1:n.1635+465C>T
XM_017011052.1:c.1635+465C>T XP_016866541.1:n.1635+465C>T
XM_017011053.1:c.1635+465C>T XP_016866542.1:n.1635+465C>T
XM_017011054.1:c.1635+465C>T XP_016866543.1:n.1635+465C>T
XM_017011055.1:c.198+465C>T XP_016866544.1:n.198+465C>T