Canonical Allele Identifier: CA823788926

Gene: TRIM10

Linked Data

• dbSNP Id: rs1205011997
• MyVariant Identifiers: chr6:g.30119794A>G (hg19) ; chr6:g.30152017A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30152017A>G , CM000668.2:g.30152017A>G	GRCh38
NC_000006.11:g.30119794A>G , CM000668.1:g.30119794A>G	GRCh37
NC_000006.10:g.30227773A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000449742.7:c.*1952T>C MANE Select	ENSP00000397073.2:n.*1952T>C
ENST00000376704.3:c.*1671T>C	ENSP00000365894.3:n.*1671T>C
ENST00000449742.6:c.*1952T>C	ENSP00000397073.2:n.*1952T>C
NM_006778.3:c.*1952T>C	NP_006769.2:n.*1952T>C
NM_052828.2:c.*1671T>C	NP_439893.2:n.*1671T>C
XM_011514221.1:c.*1952T>C	XP_011512523.1:n.*1952T>C
XM_011514222.1:c.*1952T>C	XP_011512524.1:n.*1952T>C
XM_011514223.1:c.*1952T>C	XP_011512525.1:n.*1952T>C
XM_011514224.1:c.*1952T>C	XP_011512526.1:n.*1952T>C
XM_011514225.1:c.*1671T>C	XP_011512527.1:n.*1671T>C
XM_011514222.2:c.*1952T>C	XP_011512524.1:n.*1952T>C
XM_011514223.2:c.*1952T>C	XP_011512525.1:n.*1952T>C
NM_006778.4:c.*1952T>C MANE Select	NP_006769.2:n.*1952T>C
NM_052828.3:c.*1671T>C	NP_439893.2:n.*1671T>C