Canonical Allele Identifier: CA1504297354

Gene: TRIM2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.153159661C>A , CM000666.2:g.153159661C>A	GRCh38
NC_000004.11:g.154080813C>A , CM000666.1:g.154080813C>A	GRCh37
NC_000004.10:g.154300263C>A	NCBI36
NG_041788.1:g.11544C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437508.7:c.-49+6391C>A	ENSP00000415812.2:n.-49+6391C>A
ENST00000674874.1:c.-52+7049C>A	ENSP00000502519.1:n.-52+7049C>A
ENST00000675315.1:c.-49+7049C>A	ENSP00000502676.1:n.-49+7049C>A
ENST00000675518.1:c.-52+7049C>A	ENSP00000501852.1:n.-52+7049C>A
ENST00000675745.1:c.-49+7044C>A	ENSP00000501662.1:n.-49+7044C>A
ENST00000675782.1:c.-125+6391C>A	ENSP00000502776.1:n.-125+6391C>A
ENST00000676348.1:c.-49+6391C>A	ENSP00000502159.1:n.-49+6391C>A
ENST00000676408.1:c.-49+7049C>A	ENSP00000502077.1:n.-49+7049C>A
ENST00000676423.1:c.-49+7379C>A	ENSP00000501612.1:n.-49+7379C>A
ENST00000676458.1:c.-52+6391C>A	ENSP00000501994.1:n.-52+6391C>A
ENST00000437508.6:c.-49+6391C>A	ENSP00000415812.2:n.-49+6391C>A
ENST00000441616.5:c.-49+7049C>A	ENSP00000400879.1:n.-49+7049C>A
NM_001130067.1:c.-49+6391C>A	NP_001123539.1:n.-49+6391C>A
XM_011531796.1:c.-52+7049C>A	XP_011530098.1:n.-52+7049C>A
XM_011531798.1:c.-49+7049C>A	XP_011530100.1:n.-49+7049C>A
NM_001351056.1:c.-49+7049C>A	NP_001337985.1:n.-49+7049C>A
XM_011531796.3:c.-52+7049C>A	XP_011530098.1:n.-52+7049C>A
XM_017007948.2:c.-52+7049C>A	XP_016863437.1:n.-52+7049C>A
XM_017007951.1:c.-49+7049C>A	XP_016863440.1:n.-49+7049C>A
XM_017007952.1:c.-49+7044C>A	XP_016863441.1:n.-49+7044C>A
NM_001130067.2:c.-49+6391C>A	NP_001123539.1:n.-49+6391C>A
NM_001351056.2:c.-49+7049C>A	NP_001337985.1:n.-49+7049C>A
NM_001375513.1:c.-49+7049C>A	NP_001362442.1:n.-49+7049C>A
NM_001375514.1:c.-49+7044C>A	NP_001362443.1:n.-49+7044C>A
NM_001375515.1:c.-52+6391C>A	NP_001362444.1:n.-52+6391C>A
NM_001375517.1:c.-49+7379C>A	NP_001362446.1:n.-49+7379C>A
NM_001375525.1:c.-125+6391C>A	NP_001362454.1:n.-125+6391C>A