Canonical Allele Identifier: CA7868885
Gene: TRAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3717472G>A , CM000678.2:g.3717472G>A GRCh38
NC_000016.9:g.3767473G>A , CM000678.1:g.3767473G>A GRCh37
NC_000016.8:g.3707474G>A NCBI36
NG_033088.1:g.5126C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000246957.10:c.37C>T MANE Select ENSP00000246957.5:p.Arg13Cys
ENST00000246957.9:c.37C>T ENSP00000246957.5:p.Arg13Cys
ENST00000538171.5:c.37C>T ENSP00000442070.1:p.Arg13Cys
ENST00000570403.1:c.37C>T ENSP00000461354.1:p.Arg13Cys
ENST00000571011.1:c.37C>T ENSP00000460545.1:p.Arg13Cys
ENST00000571804.5:c.37C>T ENSP00000461618.1:p.Arg13Cys
ENST00000574941.5:n.55C>T
ENST00000576106.5:n.82C>T
NM_001272049.1:c.37C>T NP_001258978.1:p.Arg13Cys
NM_016292.2:c.37C>T NP_057376.2:p.Arg13Cys
NM_016292.3:c.37C>T MANE Select NP_057376.2:p.Arg13Cys
NM_001272049.2:c.37C>T NP_001258978.1:p.Arg13Cys