Canonical Allele Identifier: CA4360716

Gene: TRRAP

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.98956157G>T , CM000669.2:g.98956157G>T	GRCh38
NC_000007.13:g.98553780G>T , CM000669.1:g.98553780G>T	GRCh37
NC_000007.12:g.98391716G>T	NCBI36
NG_030010.1:g.82668G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001375524.1:c.5949G>T MANE Select	NP_001362453.1:p.Pro1983=
ENST00000456197.2:c.5949G>T MANE Select	ENSP00000394645.2:p.Pro1983=
NM_001244580.1:c.5928G>T	NP_001231509.1:p.Pro1976=
NM_001244580.2:c.5928G>T	NP_001231509.1:p.Pro1976=
NM_003496.3:c.5874G>T	NP_003487.1:p.Pro1958=
NM_003496.4:c.5874G>T	NP_003487.1:p.Pro1958=
ENST00000355540.7:c.5874G>T	ENSP00000347733.3:p.Pro1958=
ENST00000359863.8:c.5928G>T	ENSP00000352925.4:p.Pro1976=
ENST00000446306.7:c.5871G>T	ENSP00000403708.3:p.Pro1957=
ENST00000446306.8:c.5871G>T	ENSP00000403708.3:p.Pro1957=
ENST00000456197.1:c.5093G>T
ENST00000628380.2:c.5871G>T	ENSP00000485781.1:p.Pro1957=
ENST00000704588.1:c.1686G>T	ENSP00000515962.1:p.Pro562=