Canonical Allele Identifier: CA2677825991

Gene: TRIM10

Linked Data

• gnomAD v4: 6-30152131-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30152131A>G , CM000668.2:g.30152131A>G	GRCh38
NC_000006.11:g.30119908A>G , CM000668.1:g.30119908A>G	GRCh37
NC_000006.10:g.30227887A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000449742.7:c.*1838T>C MANE Select	ENSP00000397073.2:n.*1838T>C
ENST00000376704.3:c.*1557T>C	ENSP00000365894.3:n.*1557T>C
ENST00000449742.6:c.*1838T>C	ENSP00000397073.2:n.*1838T>C
NM_006778.3:c.*1838T>C	NP_006769.2:n.*1838T>C
NM_052828.2:c.*1557T>C	NP_439893.2:n.*1557T>C
XM_011514221.1:c.*1838T>C	XP_011512523.1:n.*1838T>C
XM_011514222.1:c.*1838T>C	XP_011512524.1:n.*1838T>C
XM_011514223.1:c.*1838T>C	XP_011512525.1:n.*1838T>C
XM_011514224.1:c.*1838T>C	XP_011512526.1:n.*1838T>C
XM_011514225.1:c.*1557T>C	XP_011512527.1:n.*1557T>C
XM_011514222.2:c.*1838T>C	XP_011512524.1:n.*1838T>C
XM_011514223.2:c.*1838T>C	XP_011512525.1:n.*1838T>C
NM_006778.4:c.*1838T>C MANE Select	NP_006769.2:n.*1838T>C
NM_052828.3:c.*1557T>C	NP_439893.2:n.*1557T>C