Canonical Allele Identifier: CA2677826004

Gene: TRIM10

Linked Data

• gnomAD v4: 6-30152151-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30152151G>T , CM000668.2:g.30152151G>T	GRCh38
NC_000006.11:g.30119928G>T , CM000668.1:g.30119928G>T	GRCh37
NC_000006.10:g.30227907G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000449742.7:c.*1818C>A MANE Select	ENSP00000397073.2:n.*1818C>A
ENST00000376704.3:c.*1537C>A	ENSP00000365894.3:n.*1537C>A
ENST00000449742.6:c.*1818C>A	ENSP00000397073.2:n.*1818C>A
NM_006778.3:c.*1818C>A	NP_006769.2:n.*1818C>A
NM_052828.2:c.*1537C>A	NP_439893.2:n.*1537C>A
XM_011514221.1:c.*1818C>A	XP_011512523.1:n.*1818C>A
XM_011514222.1:c.*1818C>A	XP_011512524.1:n.*1818C>A
XM_011514223.1:c.*1818C>A	XP_011512525.1:n.*1818C>A
XM_011514224.1:c.*1818C>A	XP_011512526.1:n.*1818C>A
XM_011514225.1:c.*1537C>A	XP_011512527.1:n.*1537C>A
XM_011514222.2:c.*1818C>A	XP_011512524.1:n.*1818C>A
XM_011514223.2:c.*1818C>A	XP_011512525.1:n.*1818C>A
NM_006778.4:c.*1818C>A MANE Select	NP_006769.2:n.*1818C>A
NM_052828.3:c.*1537C>A	NP_439893.2:n.*1537C>A