Canonical Allele Identifier: CA136069214

Gene: TRIM10

Linked Data

• dbSNP Id: rs10733
• MyVariant Identifiers: chr6:g.30119796G>A (hg19) ; chr6:g.30152019G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30152019G>A , CM000668.2:g.30152019G>A	GRCh38
NC_000006.11:g.30119796G>A , CM000668.1:g.30119796G>A	GRCh37
NC_000006.10:g.30227775G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000449742.7:c.*1950C>T MANE Select	ENSP00000397073.2:n.*1950C>T
ENST00000376704.3:c.*1669C>T	ENSP00000365894.3:n.*1669C>T
ENST00000449742.6:c.*1950C>T	ENSP00000397073.2:n.*1950C>T
NM_006778.3:c.*1950C>T	NP_006769.2:n.*1950C>T
NM_052828.2:c.*1669C>T	NP_439893.2:n.*1669C>T
XM_011514221.1:c.*1950C>T	XP_011512523.1:n.*1950C>T
XM_011514222.1:c.*1950C>T	XP_011512524.1:n.*1950C>T
XM_011514223.1:c.*1950C>T	XP_011512525.1:n.*1950C>T
XM_011514224.1:c.*1950C>T	XP_011512526.1:n.*1950C>T
XM_011514225.1:c.*1669C>T	XP_011512527.1:n.*1669C>T
XM_011514222.2:c.*1950C>T	XP_011512524.1:n.*1950C>T
XM_011514223.2:c.*1950C>T	XP_011512525.1:n.*1950C>T
NM_006778.4:c.*1950C>T MANE Select	NP_006769.2:n.*1950C>T
NM_052828.3:c.*1669C>T	NP_439893.2:n.*1669C>T