Canonical Allele Identifier: CA823775244

Gene: TRIM10

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449742.7:c.-314C>T MANE Select	ENSP00000397073.2:n.-314C>T
XM_011514221.1:c.110C>T	XP_011512523.1:p.Ser37Phe
XM_011514222.1:c.110C>T	XP_011512524.1:p.Ser37Phe
XM_011514223.1:c.110C>T	XP_011512525.1:p.Ser37Phe
XM_011514224.1:c.110C>T	XP_011512526.1:p.Ser37Phe
XM_011514225.1:c.110C>T	XP_011512527.1:p.Ser37Phe
XM_011514222.2:c.110C>T	XP_011512524.1:p.Ser37Phe
XM_011514223.2:c.110C>T	XP_011512525.1:p.Ser37Phe
NM_006778.4:c.-314C>T MANE Select	NP_006769.2:n.-314C>T
NM_052828.3:c.-314C>T	NP_439893.2:n.-314C>T