Canonical Allele Identifier: CA368343574

Gene: TRRAP

Linked Data

• ClinVar Variation Id: 2582431
• ClinVar RCV Id: RCV003333417 ; RCV003333416
• dbSNP Id: rs1212619468
• gnomAD v4: 7-99011489-C-T
• MyVariant Identifiers: chr7:g.98609112C>T (hg19) ; chr7:g.99011489C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99011489C>T , CM000669.2:g.99011489C>T	GRCh38
NC_000007.13:g.98609112C>T , CM000669.1:g.98609112C>T	GRCh37
NC_000007.12:g.98447048C>T	NCBI36
NG_030010.1:g.138000C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446306.8:c.11216C>T	ENSP00000403708.3:p.Ala3739Val
ENST00000704588.1:c.6766C>T	ENSP00000515962.1:n.6766C>T
ENST00000704590.1:c.2195C>T	ENSP00000515964.1:p.Ala732Val
ENST00000704591.1:c.883-582C>T	ENSP00000515965.1:n.883-582C>T
ENST00000360902.2:c.3704C>T	ENSP00000496512.1:p.Ala1235Val
ENST00000456197.2:c.11291C>T MANE Select	ENSP00000394645.2:p.Ala3764Val
ENST00000355540.7:c.11162C>T	ENSP00000347733.3:p.Ala3721Val
ENST00000359863.8:c.11249C>T	ENSP00000352925.4:p.Ala3750Val
ENST00000446306.7:c.11216C>T	ENSP00000403708.3:p.Ala3739Val
ENST00000456197.1:c.10435C>T
ENST00000628380.2:c.11216C>T	ENSP00000485781.1:p.Ala3739Val
NM_001244580.1:c.11249C>T	NP_001231509.1:p.Ala3750Val
NM_003496.3:c.11162C>T	NP_003487.1:p.Ala3721Val
NM_001375524.1:c.11291C>T MANE Select	NP_001362453.1:p.Ala3764Val
NM_001244580.2:c.11249C>T	NP_001231509.1:p.Ala3750Val
NM_003496.4:c.11162C>T	NP_003487.1:p.Ala3721Val