Canonical Allele Identifier: CA501845632

Gene: TRIM47

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75876867A>C , CM000679.2:g.75876867A>C	GRCh38
NC_000017.10:g.73872948A>C , CM000679.1:g.73872948A>C	GRCh37
NC_000017.9:g.71384543A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254816.6:c.676-54T>G MANE Select	ENSP00000254816.1:n.676-54T>G
ENST00000254816.5:c.676-54T>G	ENSP00000254816.1:n.676-54T>G
ENST00000586495.1:c.-93T>G	ENSP00000465038.1:n.-93T>G
ENST00000587339.2:c.347-54T>G
ENST00000587774.1:n.341-54T>G
NM_033452.2:c.676-54T>G	NP_258411.2:n.676-54T>G
XM_005257787.3:c.-39-54T>G	XP_005257844.1:n.-39-54T>G
XM_005257788.3:c.-39-54T>G	XP_005257845.1:n.-39-54T>G
XM_005257787.4:c.-39-54T>G	XP_005257844.1:n.-39-54T>G
XM_005257788.5:c.-39-54T>G	XP_005257845.1:n.-39-54T>G
NM_033452.3:c.676-54T>G MANE Select	NP_258411.2:n.676-54T>G