Canonical Allele Identifier: CA368299142

Gene: TRRAP

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.98930144G>A , CM000669.2:g.98930144G>A	GRCh38
NC_000007.13:g.98527767G>A , CM000669.1:g.98527767G>A	GRCh37
NC_000007.12:g.98365703G>A	NCBI36
NG_030010.1:g.56655G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001375524.1:c.3331G>A MANE Select	NP_001362453.1:p.Gly1111Arg
ENST00000456197.2:c.3331G>A MANE Select	ENSP00000394645.2:p.Gly1111Arg
NM_001244580.1:c.3331G>A	NP_001231509.1:p.Gly1111Arg
NM_001244580.2:c.3331G>A	NP_001231509.1:p.Gly1111Arg
NM_003496.3:c.3331G>A	NP_003487.1:p.Gly1111Arg
NM_003496.4:c.3331G>A	NP_003487.1:p.Gly1111Arg
ENST00000355540.7:c.3331G>A	ENSP00000347733.3:p.Gly1111Arg
ENST00000359863.8:c.3331G>A	ENSP00000352925.4:p.Gly1111Arg
ENST00000446306.7:c.3328G>A	ENSP00000403708.3:p.Gly1110Arg
ENST00000446306.8:c.3328G>A	ENSP00000403708.3:p.Gly1110Arg
ENST00000456197.1:c.2475G>A
ENST00000628380.2:c.3328G>A	ENSP00000485781.1:p.Gly1110Arg
ENST00000704587.1:c.3220G>A	ENSP00000515961.1:p.Gly1074Arg