Canonical Allele Identifier: CA1618610444

Gene: TRIM10

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30152047A= , CM000668.2:g.30152047A=	GRCh38
NC_000006.11:g.30119824A= , CM000668.1:g.30119824A=	GRCh37
NC_000006.10:g.30227803A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000449742.7:c.*1922T= MANE Select	ENSP00000397073.2:n.*1922T=
ENST00000376704.3:c.*1641T=	ENSP00000365894.3:n.*1641T=
ENST00000449742.6:c.*1922T=	ENSP00000397073.2:n.*1922T=
NM_006778.3:c.*1922T=	NP_006769.2:n.*1922T=
NM_052828.2:c.*1641T=	NP_439893.2:n.*1641T=
XM_011514221.1:c.*1922T=	XP_011512523.1:n.*1922T=
XM_011514222.1:c.*1922T=	XP_011512524.1:n.*1922T=
XM_011514223.1:c.*1922T=	XP_011512525.1:n.*1922T=
XM_011514224.1:c.*1922T=	XP_011512526.1:n.*1922T=
XM_011514225.1:c.*1641T=	XP_011512527.1:n.*1641T=
XM_011514222.2:c.*1922T=	XP_011512524.1:n.*1922T=
XM_011514223.2:c.*1922T=	XP_011512525.1:n.*1922T=
NM_006778.4:c.*1922T= MANE Select	NP_006769.2:n.*1922T=
NM_052828.3:c.*1641T=	NP_439893.2:n.*1641T=