Canonical Allele Identifier: CA136069249

Gene: TRIM10

Linked Data

• dbSNP Id: rs902185994
• gnomAD v3: 6-30152086-G-T
• gnomAD v4: 6-30152086-G-T
• MyVariant Identifiers: chr6:g.30119863G>T (hg19) ; chr6:g.30152086G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30152086G>T , CM000668.2:g.30152086G>T	GRCh38
NC_000006.11:g.30119863G>T , CM000668.1:g.30119863G>T	GRCh37
NC_000006.10:g.30227842G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000449742.7:c.*1883C>A MANE Select	ENSP00000397073.2:n.*1883C>A
ENST00000376704.3:c.*1602C>A	ENSP00000365894.3:n.*1602C>A
ENST00000449742.6:c.*1883C>A	ENSP00000397073.2:n.*1883C>A
NM_006778.3:c.*1883C>A	NP_006769.2:n.*1883C>A
NM_052828.2:c.*1602C>A	NP_439893.2:n.*1602C>A
XM_011514221.1:c.*1883C>A	XP_011512523.1:n.*1883C>A
XM_011514222.1:c.*1883C>A	XP_011512524.1:n.*1883C>A
XM_011514223.1:c.*1883C>A	XP_011512525.1:n.*1883C>A
XM_011514224.1:c.*1883C>A	XP_011512526.1:n.*1883C>A
XM_011514225.1:c.*1602C>A	XP_011512527.1:n.*1602C>A
XM_011514222.2:c.*1883C>A	XP_011512524.1:n.*1883C>A
XM_011514223.2:c.*1883C>A	XP_011512525.1:n.*1883C>A
NM_006778.4:c.*1883C>A MANE Select	NP_006769.2:n.*1883C>A
NM_052828.3:c.*1602C>A	NP_439893.2:n.*1602C>A