Canonical Allele Identifier: CA377932957

Gene: TRIM8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102657218C>T , CM000672.2:g.102657218C>T	GRCh38
NC_000010.10:g.104416975C>T , CM000672.1:g.104416975C>T	GRCh37
NC_000010.9:g.104406965C>T	NCBI36
NG_051595.1:g.17724C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_030912.3:c.1520C>T MANE Select	NP_112174.2:p.Pro507Leu
ENST00000643721.2:c.1520C>T MANE Select	ENSP00000496301.1:p.Pro507Leu
NM_001345950.1:c.1424C>T	NP_001332879.1:p.Pro475Leu
NM_030912.2:c.1520C>T	NP_112174.2:p.Pro507Leu
NR_144321.1:n.1668C>T
ENST00000302424.11:c.1520C>T	ENSP00000302120.5:p.Pro507Leu
ENST00000302424.12:c.*699C>T	ENSP00000302120.6:n.*699C>T
ENST00000642664.1:c.1323C>T	ENSP00000496615.1:n.1323C>T
ENST00000643100.1:c.444-705C>T
ENST00000643376.1:c.1157C>T
ENST00000644572.1:n.1969C>T
ENST00000644914.1:c.246-832C>T	ENSP00000494335.1:n.246-832C>T
ENST00000646757.1:n.1559C>T
ENST00000710327.1:c.1520C>T	ENSP00000518207.1:p.Pro507Leu
XM_011540217.1:c.1424C>T	XP_011538519.1:p.Pro475Leu