Canonical Allele Identifier: CA2581557840

Gene: TRIM10

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449742.7:c.-314C>G MANE Select	ENSP00000397073.2:n.-314C>G
XM_011514221.1:c.110C>G	XP_011512523.1:p.Ser37Cys
XM_011514222.1:c.110C>G	XP_011512524.1:p.Ser37Cys
XM_011514223.1:c.110C>G	XP_011512525.1:p.Ser37Cys
XM_011514224.1:c.110C>G	XP_011512526.1:p.Ser37Cys
XM_011514225.1:c.110C>G	XP_011512527.1:p.Ser37Cys
XM_011514222.2:c.110C>G	XP_011512524.1:p.Ser37Cys
XM_011514223.2:c.110C>G	XP_011512525.1:p.Ser37Cys
NM_006778.4:c.-314C>G MANE Select	NP_006769.2:n.-314C>G
NM_052828.3:c.-314C>G	NP_439893.2:n.-314C>G