Canonical Allele Identifier: CA1932763928

Gene: TRIM8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102654464A= , CM000672.2:g.102654464A=	GRCh38
NC_000010.10:g.104414221A= , CM000672.1:g.104414221A=	GRCh37
NC_000010.9:g.104404211A=	NCBI36
NG_051595.1:g.14970A=

Transcript Alleles

HGVS	Amino-acid Change
NM_030912.3:c.571-189A= MANE Select	NP_112174.2:n.571-189A=
ENST00000643721.2:c.571-189A= MANE Select	ENSP00000496301.1:n.571-189A=
NM_001345950.1:c.571-616A=	NP_001332879.1:n.571-616A=
NM_030912.2:c.571-189A=	NP_112174.2:n.571-189A=
NR_144321.1:n.694-189A=
ENST00000302424.11:c.571-189A=	ENSP00000302120.5:n.571-189A=
ENST00000302424.12:c.571-189A=	ENSP00000302120.6:n.571-189A=
ENST00000462202.2:c.302-616A=
ENST00000462202.3:c.302-616A=
ENST00000479004.2:n.152-189A=
ENST00000487927.5:n.61-189A=
ENST00000487927.6:n.68-189A=
ENST00000642664.1:c.352-189A=	ENSP00000496615.1:n.352-189A=
ENST00000643376.1:c.183-189A=
ENST00000644572.1:n.500A=
ENST00000644979.1:n.1004A=
ENST00000645961.1:c.181-189A=	ENSP00000494181.1:n.181-189A=
ENST00000646349.1:n.126-189A=
ENST00000646757.1:n.421A=
ENST00000710327.1:c.571-189A=	ENSP00000518207.1:n.571-189A=
XM_006717988.2:c.571-189A=	XP_006718051.1:n.571-189A=
XM_011540217.1:c.571-616A=	XP_011538519.1:n.571-616A=
XR_001747575.1:n.85+583T=
XR_001747576.1:n.85+583T=
XR_946271.1:n.85+583T=
XR_946272.1:n.85+583T=