Canonical Allele Identifier: CA358675431

Gene: TRIM61 FAM218A

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.164957183A>T , CM000666.2:g.164957183A>T	GRCh38
NC_000004.11:g.165878335A>T , CM000666.1:g.165878335A>T	GRCh37
NC_000004.10:g.166097785A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329314.6:c.526-2087T>A (TRIM61)	ENSP00000332288.5:n.526-2087T>A
ENST00000329314.5:c.526-2087T>A (TRIM61)	ENSP00000332288.5:n.526-2087T>A
ENST00000513876.3:c.161A>T (FAM218A)	ENSP00000427428.1:p.His54Leu
ENST00000616332.1:c.526-2087T>A (TRIM61)	ENSP00000482389.1:n.526-2087T>A
NM_001012414.2:c.526-2087T>A (TRIM61)	NP_001012414.1:n.526-2087T>A
NM_153027.1:c.161A>T (FAM218A)	NP_694572.1:p.His54Leu
NM_153027.2:c.161A>T (FAM218A)	NP_694572.1:p.His54Leu
NM_001012414.3:c.526-2087T>A (TRIM61)	NP_001012414.1:n.526-2087T>A
NR_160935.1:n.236A>T (FAM218A)