Canonical Allele Identifier: CA823788948

Gene: TRIM10

Linked Data

• dbSNP Id: rs1160297288
• MyVariant Identifiers: chr6:g.30119858C>T (hg19) ; chr6:g.30152081C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30152081C>T , CM000668.2:g.30152081C>T	GRCh38
NC_000006.11:g.30119858C>T , CM000668.1:g.30119858C>T	GRCh37
NC_000006.10:g.30227837C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000449742.7:c.*1888G>A MANE Select	ENSP00000397073.2:n.*1888G>A
ENST00000376704.3:c.*1607G>A	ENSP00000365894.3:n.*1607G>A
ENST00000449742.6:c.*1888G>A	ENSP00000397073.2:n.*1888G>A
NM_006778.3:c.*1888G>A	NP_006769.2:n.*1888G>A
NM_052828.2:c.*1607G>A	NP_439893.2:n.*1607G>A
XM_011514221.1:c.*1888G>A	XP_011512523.1:n.*1888G>A
XM_011514222.1:c.*1888G>A	XP_011512524.1:n.*1888G>A
XM_011514223.1:c.*1888G>A	XP_011512525.1:n.*1888G>A
XM_011514224.1:c.*1888G>A	XP_011512526.1:n.*1888G>A
XM_011514225.1:c.*1607G>A	XP_011512527.1:n.*1607G>A
XM_011514222.2:c.*1888G>A	XP_011512524.1:n.*1888G>A
XM_011514223.2:c.*1888G>A	XP_011512525.1:n.*1888G>A
NM_006778.4:c.*1888G>A MANE Select	NP_006769.2:n.*1888G>A
NM_052828.3:c.*1607G>A	NP_439893.2:n.*1607G>A