Canonical Allele Identifier: CA1528724141

Gene: TRIO

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14393640_14393642delinsGTG , CM000667.2:g.14393640_14393642delinsGTG	GRCh38
NC_000005.9:g.14393749_14393751delinsGTG , CM000667.1:g.14393749_14393751delinsGTG	GRCh37
NC_000005.8:g.14446749_14446751delinsGTG	NCBI36
NG_052962.1:g.254939_254941delinsGTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000698541.1:c.4219-398_4219-396delinsGTG	ENSP00000513786.1:n.4219-398_4219-396delinsGTG
ENST00000344204.9:c.4219-398_4219-396delinsGTG MANE Select	ENSP00000339299.4:n.4219-398_4219-396delinsGTG
ENST00000344204.8:c.4219-398_4219-396delinsGTG	ENSP00000339299.4:n.4219-398_4219-396delinsGTG
ENST00000502490.1:n.407-398_407-396delinsGTG
ENST00000509967.6:c.4072-398_4072-396delinsGTG	ENSP00000445592.1:n.4072-398_4072-396delinsGTG
ENST00000512070.6:c.4042-398_4042-396delinsGTG	ENSP00000421555.2:n.4042-398_4042-396delinsGTG
ENST00000513206.5:c.3418-398_3418-396delinsGTG	ENSP00000426342.2:n.3418-398_3418-396delinsGTG
ENST00000515144.5:n.3137-398_3137-396delinsGTG
NM_007118.2:c.4219-398_4219-396delinsGTG	NP_009049.2:n.4219-398_4219-396delinsGTG
XM_011514107.1:c.4156-398_4156-396delinsGTG	XP_011512409.1:n.4156-398_4156-396delinsGTG
XM_011514108.1:c.4102-398_4102-396delinsGTG	XP_011512410.1:n.4102-398_4102-396delinsGTG
XM_011514109.1:c.4072-398_4072-396delinsGTG	XP_011512411.1:n.4072-398_4072-396delinsGTG
XM_011514110.1:c.4042-398_4042-396delinsGTG	XP_011512412.1:n.4042-398_4042-396delinsGTG
XM_011514111.1:c.4042-398_4042-396delinsGTG	XP_011512413.1:n.4042-398_4042-396delinsGTG
XM_011514112.1:c.2764-398_2764-396delinsGTG	XP_011512414.1:n.2764-398_2764-396delinsGTG
XM_011514113.1:c.4219-398_4219-396delinsGTG	XP_011512415.1:n.4219-398_4219-396delinsGTG
XR_241714.1:n.4237-398_4237-396delinsGTG
NM_007118.3:c.4219-398_4219-396delinsGTG	NP_009049.2:n.4219-398_4219-396delinsGTG
NR_134469.1:n.4243-398_4243-396delinsGTG
XM_011514107.2:c.4156-398_4156-396delinsGTG	XP_011512409.1:n.4156-398_4156-396delinsGTG
XM_011514109.3:c.4072-398_4072-396delinsGTG	XP_011512411.1:n.4072-398_4072-396delinsGTG
XM_011514110.3:c.4042-398_4042-396delinsGTG	XP_011512412.1:n.4042-398_4042-396delinsGTG
XM_017009801.1:c.4219-398_4219-396delinsGTG	XP_016865290.1:n.4219-398_4219-396delinsGTG
XM_017009802.1:c.4219-398_4219-396delinsGTG	XP_016865291.1:n.4219-398_4219-396delinsGTG
XM_017009803.1:c.2764-398_2764-396delinsGTG	XP_016865292.1:n.2764-398_2764-396delinsGTG
XR_001742236.2:n.4595-398_4595-396delinsGTG
NM_007118.4:c.4219-398_4219-396delinsGTG MANE Select	NP_009049.2:n.4219-398_4219-396delinsGTG
NR_134469.2:n.4603-398_4603-396delinsGTG