Canonical Allele Identifier: CA7868372

Gene: TRAP1 DNASE1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3674427G>A , CM000678.2:g.3674427G>A	GRCh38
NC_000016.9:g.3724428G>A , CM000678.1:g.3724428G>A	GRCh37
NC_000016.8:g.3664429G>A	NCBI36
NG_033088.1:g.48171C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246957.10:c.956C>T (TRAP1) MANE Select	ENSP00000246957.5:p.Ala319Val
ENST00000246957.9:c.956C>T (TRAP1)	ENSP00000246957.5:p.Ala319Val
ENST00000538171.5:c.797C>T (TRAP1)	ENSP00000442070.1:p.Ala266Val
ENST00000570514.5:n.321C>T (TRAP1)
ENST00000573872.5:n.405C>T (TRAP1)
ENST00000574175.1:c.428C>T (TRAP1)
ENST00000575479.1:c.219-5322G>A (DNASE1)
ENST00000575671.5:c.329C>T (TRAP1)	ENSP00000458166.1:p.Ala110Val
ENST00000576335.5:c.329C>T (TRAP1)	ENSP00000459354.1:p.Ala110Val
NM_001272049.1:c.797C>T (TRAP1)	NP_001258978.1:p.Ala266Val
NM_016292.2:c.956C>T (TRAP1)	NP_057376.2:p.Ala319Val
XM_011522345.1:c.536C>T (TRAP1)	XP_011520647.1:p.Ala179Val
XM_011522345.2:c.536C>T (TRAP1)	XP_011520647.1:p.Ala179Val
NM_016292.3:c.956C>T (TRAP1) MANE Select	NP_057376.2:p.Ala319Val
NM_001272049.2:c.797C>T (TRAP1)	NP_001258978.1:p.Ala266Val