Canonical Allele Identifier: CA2838355976

Gene: TRIM8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102649267G>T , CM000672.2:g.102649267G>T	GRCh38
NC_000010.10:g.104409024G>T , CM000672.1:g.104409024G>T	GRCh37
NC_000010.9:g.104399014G>T	NCBI36
NG_051595.1:g.9773G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710327.1:c.570+4080G>T	ENSP00000518207.1:n.570+4080G>T
ENST00000302424.12:c.570+4080G>T	ENSP00000302120.6:n.570+4080G>T
ENST00000462202.3:c.301+4080G>T
ENST00000479004.2:n.151+3864G>T
ENST00000487927.6:n.56G>T
ENST00000642664.1:c.351+4080G>T	ENSP00000496615.1:n.351+4080G>T
ENST00000643376.1:c.182+4080G>T
ENST00000643721.2:c.570+4080G>T MANE Select	ENSP00000496301.1:n.570+4080G>T
ENST00000645961.1:c.180+4080G>T	ENSP00000494181.1:n.180+4080G>T
ENST00000646349.1:n.125+3446G>T
ENST00000302424.11:c.570+4080G>T	ENSP00000302120.5:n.570+4080G>T
ENST00000462202.2:c.301+4080G>T
ENST00000487927.5:n.49G>T
NM_030912.2:c.570+4080G>T	NP_112174.2:n.570+4080G>T
XM_006717988.2:c.570+4080G>T	XP_006718051.1:n.570+4080G>T
XM_011540217.1:c.570+4080G>T	XP_011538519.1:n.570+4080G>T
NM_001345950.1:c.570+4080G>T	NP_001332879.1:n.570+4080G>T
NR_144321.1:n.693+4080G>T
NM_030912.3:c.570+4080G>T MANE Select	NP_112174.2:n.570+4080G>T