Canonical Allele Identifier: CA1528724044

Gene: TRIO

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14393436C= , CM000667.2:g.14393436C=	GRCh38
NC_000005.9:g.14393545C= , CM000667.1:g.14393545C=	GRCh37
NC_000005.8:g.14446545C=	NCBI36
NG_052962.1:g.254735C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000698541.1:c.4219-602C=	ENSP00000513786.1:n.4219-602C=
ENST00000344204.9:c.4219-602C= MANE Select	ENSP00000339299.4:n.4219-602C=
ENST00000344204.8:c.4219-602C=	ENSP00000339299.4:n.4219-602C=
ENST00000502490.1:n.407-602C=
ENST00000509967.6:c.4072-602C=	ENSP00000445592.1:n.4072-602C=
ENST00000512070.6:c.4042-602C=	ENSP00000421555.2:n.4042-602C=
ENST00000513206.5:c.3418-602C=	ENSP00000426342.2:n.3418-602C=
ENST00000515144.5:n.3137-602C=
NM_007118.2:c.4219-602C=	NP_009049.2:n.4219-602C=
XM_011514107.1:c.4156-602C=	XP_011512409.1:n.4156-602C=
XM_011514108.1:c.4102-602C=	XP_011512410.1:n.4102-602C=
XM_011514109.1:c.4072-602C=	XP_011512411.1:n.4072-602C=
XM_011514110.1:c.4042-602C=	XP_011512412.1:n.4042-602C=
XM_011514111.1:c.4042-602C=	XP_011512413.1:n.4042-602C=
XM_011514112.1:c.2764-602C=	XP_011512414.1:n.2764-602C=
XM_011514113.1:c.4219-602C=	XP_011512415.1:n.4219-602C=
XR_241714.1:n.4237-602C=
NM_007118.3:c.4219-602C=	NP_009049.2:n.4219-602C=
NR_134469.1:n.4243-602C=
XM_011514107.2:c.4156-602C=	XP_011512409.1:n.4156-602C=
XM_011514109.3:c.4072-602C=	XP_011512411.1:n.4072-602C=
XM_011514110.3:c.4042-602C=	XP_011512412.1:n.4042-602C=
XM_017009801.1:c.4219-602C=	XP_016865290.1:n.4219-602C=
XM_017009802.1:c.4219-602C=	XP_016865291.1:n.4219-602C=
XM_017009803.1:c.2764-602C=	XP_016865292.1:n.2764-602C=
XR_001742236.2:n.4595-602C=
NM_007118.4:c.4219-602C= MANE Select	NP_009049.2:n.4219-602C=
NR_134469.2:n.4603-602C=