Canonical Allele Identifier: CA294099761

Gene: TRIM47

Linked Data

• dbSNP Id: rs755292575
• gnomAD v2: 17-73872952-G-A
• gnomAD v4: 17-75876871-G-A
• MyVariant Identifiers: chr17:g.73872952G>A (hg19) ; chr17:g.75876871G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75876871G>A , CM000679.2:g.75876871G>A	GRCh38
NC_000017.10:g.73872952G>A , CM000679.1:g.73872952G>A	GRCh37
NC_000017.9:g.71384547G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000254816.6:c.676-58C>T MANE Select	ENSP00000254816.1:n.676-58C>T
ENST00000254816.5:c.676-58C>T	ENSP00000254816.1:n.676-58C>T
ENST00000586495.1:c.-97C>T	ENSP00000465038.1:n.-97C>T
ENST00000587339.2:c.347-58C>T
ENST00000587774.1:n.341-58C>T
NM_033452.2:c.676-58C>T	NP_258411.2:n.676-58C>T
XM_005257787.3:c.-39-58C>T	XP_005257844.1:n.-39-58C>T
XM_005257788.3:c.-39-58C>T	XP_005257845.1:n.-39-58C>T
XM_005257787.4:c.-39-58C>T	XP_005257844.1:n.-39-58C>T
XM_005257788.5:c.-39-58C>T	XP_005257845.1:n.-39-58C>T
NM_033452.3:c.676-58C>T MANE Select	NP_258411.2:n.676-58C>T