Canonical Allele Identifier: CA2580615947

Gene: TRRAP

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.98917615_98917616del , CM000669.2:g.98917615_98917616del	GRCh38
NC_000007.13:g.98515238_98515239del , CM000669.1:g.98515238_98515239del	GRCh37
NC_000007.12:g.98353174_98353175del	NCBI36
NG_030010.1:g.44126_44127del

Transcript Alleles

HGVS	Amino-acid Change
NM_001375524.1:c.2558_2559del MANE Select	NP_001362453.1:p.Val853GlyfsTer?
ENST00000456197.2:c.2558_2559del MANE Select	ENSP00000394645.2:p.Val853GlyfsTer?
NM_001244580.1:c.2558_2559del	NP_001231509.1:p.Val853GlyfsTer?
NM_001244580.2:c.2558_2559del	NP_001231509.1:p.Val853GlyfsTer?
NM_003496.3:c.2558_2559del	NP_003487.1:p.Val853GlyfsTer?
NM_003496.4:c.2558_2559del	NP_003487.1:p.Val853GlyfsTer?
ENST00000355540.7:c.2558_2559del	ENSP00000347733.3:p.Val853GlyfsTer?
ENST00000359863.8:c.2558_2559del	ENSP00000352925.4:p.Val853GlyfsTer?
ENST00000446306.7:c.2555_2556del	ENSP00000403708.3:p.Val852GlyfsTer?
ENST00000446306.8:c.2555_2556del	ENSP00000403708.3:p.Val852GlyfsTer?
ENST00000456197.1:c.1702_1703del
ENST00000628380.2:c.2555_2556del	ENSP00000485781.1:p.Val852GlyfsTer?
ENST00000704587.1:c.2447_2448del	ENSP00000515961.1:p.Val816GlyfsTer?