Canonical Allele Identifier: CA368311001

Gene: TRRAP

Linked Data

• ClinVar Variation Id: 2498251
• ClinVar RCV Id: RCV003221372 ; RCV004555908
• dbSNP Id: rs1792941314
• MyVariant Identifiers: chr7:g.98579527C>T (hg19) ; chr7:g.98981904C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.98981904C>T , CM000669.2:g.98981904C>T	GRCh38
NC_000007.13:g.98579527C>T , CM000669.1:g.98579527C>T	GRCh37
NC_000007.12:g.98417463C>T	NCBI36
NG_030010.1:g.108415C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446306.8:c.8695C>T	ENSP00000403708.3:p.Arg2899Cys
ENST00000704588.1:c.4507C>T	ENSP00000515962.1:p.Arg1503Cys
ENST00000704589.1:c.388-1360C>T	ENSP00000515963.1:n.388-1360C>T
ENST00000704590.1:c.136C>T	ENSP00000515964.1:p.Arg46Cys
ENST00000360902.2:c.1183C>T	ENSP00000496512.1:p.Arg395Cys
ENST00000456197.2:c.8770C>T MANE Select	ENSP00000394645.2:p.Arg2924Cys
ENST00000355540.7:c.8695C>T	ENSP00000347733.3:p.Arg2899Cys
ENST00000359863.8:c.8749C>T	ENSP00000352925.4:p.Arg2917Cys
ENST00000446306.7:c.8695C>T	ENSP00000403708.3:p.Arg2899Cys
ENST00000456197.1:c.7914C>T
ENST00000628380.2:c.8695C>T	ENSP00000485781.1:p.Arg2899Cys
NM_001244580.1:c.8749C>T	NP_001231509.1:p.Arg2917Cys
NM_003496.3:c.8695C>T	NP_003487.1:p.Arg2899Cys
NM_001375524.1:c.8770C>T MANE Select	NP_001362453.1:p.Arg2924Cys
NM_001244580.2:c.8749C>T	NP_001231509.1:p.Arg2917Cys
NM_003496.4:c.8695C>T	NP_003487.1:p.Arg2899Cys