Canonical Allele Identifier: CA1618610441
Gene: TRIM10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30152034A= , CM000668.2:g.30152034A= GRCh38
NC_000006.11:g.30119811A= , CM000668.1:g.30119811A= GRCh37
NC_000006.10:g.30227790A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000449742.7:c.*1935T= MANE Select ENSP00000397073.2:n.*1935T=
ENST00000376704.3:c.*1654T= ENSP00000365894.3:n.*1654T=
ENST00000449742.6:c.*1935T= ENSP00000397073.2:n.*1935T=
NM_006778.3:c.*1935T= NP_006769.2:n.*1935T=
NM_052828.2:c.*1654T= NP_439893.2:n.*1654T=
XM_011514221.1:c.*1935T= XP_011512523.1:n.*1935T=
XM_011514222.1:c.*1935T= XP_011512524.1:n.*1935T=
XM_011514223.1:c.*1935T= XP_011512525.1:n.*1935T=
XM_011514224.1:c.*1935T= XP_011512526.1:n.*1935T=
XM_011514225.1:c.*1654T= XP_011512527.1:n.*1654T=
XM_011514222.2:c.*1935T= XP_011512524.1:n.*1935T=
XM_011514223.2:c.*1935T= XP_011512525.1:n.*1935T=
NM_006778.4:c.*1935T= MANE Select NP_006769.2:n.*1935T=
NM_052828.3:c.*1654T= NP_439893.2:n.*1654T=