Canonical Allele Identifier: CA359198741

Gene: TRIO

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14280387C>T , CM000667.2:g.14280387C>T	GRCh38
NC_000005.9:g.14280496C>T , CM000667.1:g.14280496C>T	GRCh37
NC_000005.8:g.14333496C>T	NCBI36
NG_052962.1:g.141686C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_007118.4:c.298C>T MANE Select	NP_009049.2:p.Arg100Ter
ENST00000344204.9:c.298C>T MANE Select	ENSP00000339299.4:p.Arg100Ter
NM_007118.2:c.298C>T	NP_009049.2:p.Arg100Ter
NM_007118.3:c.298C>T	NP_009049.2:p.Arg100Ter
NR_134469.1:n.322C>T
NR_134469.2:n.682C>T
ENST00000344204.8:c.298C>T	ENSP00000339299.4:p.Arg100Ter
ENST00000502816.1:n.322C>T
ENST00000505971.5:n.322C>T
ENST00000509967.6:c.151C>T	ENSP00000445592.1:p.Arg51Ter
ENST00000512070.6:c.121C>T	ENSP00000421555.2:p.Arg41Ter
ENST00000698541.1:c.298C>T	ENSP00000513786.1:p.Arg100Ter
ENST00000704488.1:c.169C>T	ENSP00000515916.1:p.Arg57Ter
XM_011514107.1:c.235C>T	XP_011512409.1:p.Arg79Ter
XM_011514107.2:c.235C>T	XP_011512409.1:p.Arg79Ter
XM_011514108.1:c.181C>T	XP_011512410.1:p.Arg61Ter
XM_011514109.1:c.151C>T	XP_011512411.1:p.Arg51Ter
XM_011514109.3:c.151C>T	XP_011512411.1:p.Arg51Ter
XM_011514110.1:c.121C>T	XP_011512412.1:p.Arg41Ter
XM_011514110.3:c.121C>T	XP_011512412.1:p.Arg41Ter
XM_011514111.1:c.121C>T	XP_011512413.1:p.Arg41Ter
XM_011514113.1:c.298C>T	XP_011512415.1:p.Arg100Ter
XM_017009801.1:c.298C>T	XP_016865290.1:p.Arg100Ter
XM_017009802.1:c.298C>T	XP_016865291.1:p.Arg100Ter
XR_001742236.2:n.674C>T
XR_241714.1:n.316C>T