Canonical Allele Identifier: CA136077714

Gene: TRIM10

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30161172G>T , CM000668.2:g.30161172G>T	GRCh38
NC_000006.11:g.30128949G>T , CM000668.1:g.30128949G>T	GRCh37
NC_000006.10:g.30236928G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449742.7:c.-314C>A MANE Select	ENSP00000397073.2:n.-314C>A
XM_011514221.1:c.110C>A	XP_011512523.1:p.Ser37Tyr
XM_011514222.1:c.110C>A	XP_011512524.1:p.Ser37Tyr
XM_011514223.1:c.110C>A	XP_011512525.1:p.Ser37Tyr
XM_011514224.1:c.110C>A	XP_011512526.1:p.Ser37Tyr
XM_011514225.1:c.110C>A	XP_011512527.1:p.Ser37Tyr
XM_011514222.2:c.110C>A	XP_011512524.1:p.Ser37Tyr
XM_011514223.2:c.110C>A	XP_011512525.1:p.Ser37Tyr
NM_006778.4:c.-314C>A MANE Select	NP_006769.2:n.-314C>A
NM_052828.3:c.-314C>A	NP_439893.2:n.-314C>A