Canonical Allele Identifier: CA443273880

Gene: TRIO

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14297263G>A , CM000667.2:g.14297263G>A	GRCh38
NC_000005.9:g.14297372G>A , CM000667.1:g.14297372G>A	GRCh37
NC_000005.8:g.14350372G>A	NCBI36
NG_052962.1:g.158562G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698541.1:c.1368G>A	ENSP00000513786.1:p.Lys456=
ENST00000704488.1:c.1239G>A	ENSP00000515916.1:p.Lys413=
ENST00000344204.9:c.1368G>A MANE Select	ENSP00000339299.4:p.Lys456=
ENST00000344204.8:c.1368G>A	ENSP00000339299.4:p.Lys456=
ENST00000504606.1:n.567G>A
ENST00000509967.6:c.1221G>A	ENSP00000445592.1:p.Lys407=
ENST00000512070.6:c.1191G>A	ENSP00000421555.2:p.Lys397=
ENST00000513206.5:c.567G>A	ENSP00000426342.2:p.Lys189=
ENST00000515144.5:n.286G>A
NM_007118.2:c.1368G>A	NP_009049.2:p.Lys456=
XM_011514107.1:c.1305G>A	XP_011512409.1:p.Lys435=
XM_011514108.1:c.1251G>A	XP_011512410.1:p.Lys417=
XM_011514109.1:c.1221G>A	XP_011512411.1:p.Lys407=
XM_011514110.1:c.1191G>A	XP_011512412.1:p.Lys397=
XM_011514111.1:c.1191G>A	XP_011512413.1:p.Lys397=
XM_011514113.1:c.1368G>A	XP_011512415.1:p.Lys456=
XR_241714.1:n.1386G>A
NM_007118.3:c.1368G>A	NP_009049.2:p.Lys456=
NR_134469.1:n.1392G>A
XM_011514107.2:c.1305G>A	XP_011512409.1:p.Lys435=
XM_011514109.3:c.1221G>A	XP_011512411.1:p.Lys407=
XM_011514110.3:c.1191G>A	XP_011512412.1:p.Lys397=
XM_017009801.1:c.1368G>A	XP_016865290.1:p.Lys456=
XM_017009802.1:c.1368G>A	XP_016865291.1:p.Lys456=
XR_001742236.2:n.1744G>A
NM_007118.4:c.1368G>A MANE Select	NP_009049.2:p.Lys456=
NR_134469.2:n.1752G>A