Canonical Allele Identifier: CA1528724106
Gene: TRIO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14393543_14393544delinsAC , CM000667.2:g.14393543_14393544delinsAC GRCh38
NC_000005.9:g.14393652_14393653delinsAC , CM000667.1:g.14393652_14393653delinsAC GRCh37
NC_000005.8:g.14446652_14446653delinsAC NCBI36
NG_052962.1:g.254842_254843delinsAC

Transcript Alleles

HGVS Amino-acid change
ENST00000698541.1:c.4219-495_4219-494delinsAC ENSP00000513786.1:n.4219-495_4219-494deli...
ENST00000344204.9:c.4219-495_4219-494delinsAC MANE Select ENSP00000339299.4:n.4219-495_4219-494deli...
ENST00000344204.8:c.4219-495_4219-494delinsAC ENSP00000339299.4:n.4219-495_4219-494deli...
ENST00000502490.1:n.407-495_407-494delinsAC
ENST00000509967.6:c.4072-495_4072-494delinsAC ENSP00000445592.1:n.4072-495_4072-494deli...
ENST00000512070.6:c.4042-495_4042-494delinsAC ENSP00000421555.2:n.4042-495_4042-494deli...
ENST00000513206.5:c.3418-495_3418-494delinsAC ENSP00000426342.2:n.3418-495_3418-494deli...
ENST00000515144.5:n.3137-495_3137-494delinsAC
NM_007118.2:c.4219-495_4219-494delinsAC NP_009049.2:n.4219-495_4219-494delinsAC
XM_011514107.1:c.4156-495_4156-494delinsAC XP_011512409.1:n.4156-495_4156-494delinsA...
XM_011514108.1:c.4102-495_4102-494delinsAC XP_011512410.1:n.4102-495_4102-494delinsA...
XM_011514109.1:c.4072-495_4072-494delinsAC XP_011512411.1:n.4072-495_4072-494delinsA...
XM_011514110.1:c.4042-495_4042-494delinsAC XP_011512412.1:n.4042-495_4042-494delinsA...
XM_011514111.1:c.4042-495_4042-494delinsAC XP_011512413.1:n.4042-495_4042-494delinsA...
XM_011514112.1:c.2764-495_2764-494delinsAC XP_011512414.1:n.2764-495_2764-494delinsA...
XM_011514113.1:c.4219-495_4219-494delinsAC XP_011512415.1:n.4219-495_4219-494delinsA...
XR_241714.1:n.4237-495_4237-494delinsAC
NM_007118.3:c.4219-495_4219-494delinsAC NP_009049.2:n.4219-495_4219-494delinsAC
NR_134469.1:n.4243-495_4243-494delinsAC
XM_011514107.2:c.4156-495_4156-494delinsAC XP_011512409.1:n.4156-495_4156-494delinsA...
XM_011514109.3:c.4072-495_4072-494delinsAC XP_011512411.1:n.4072-495_4072-494delinsA...
XM_011514110.3:c.4042-495_4042-494delinsAC XP_011512412.1:n.4042-495_4042-494delinsA...
XM_017009801.1:c.4219-495_4219-494delinsAC XP_016865290.1:n.4219-495_4219-494delinsA...
XM_017009802.1:c.4219-495_4219-494delinsAC XP_016865291.1:n.4219-495_4219-494delinsA...
XM_017009803.1:c.2764-495_2764-494delinsAC XP_016865292.1:n.2764-495_2764-494delinsA...
XR_001742236.2:n.4595-495_4595-494delinsAC
NM_007118.4:c.4219-495_4219-494delinsAC MANE Select NP_009049.2:n.4219-495_4219-494delinsAC
NR_134469.2:n.4603-495_4603-494delinsAC