Canonical Allele Identifier: CA2825001410

Gene: TRIO

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14471469A>G , CM000667.2:g.14471469A>G	GRCh38
NC_000005.9:g.14471578A>G , CM000667.1:g.14471578A>G	GRCh37
NC_000005.8:g.14524578A>G	NCBI36
NG_052962.1:g.332768A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698542.1:c.821+3A>G	ENSP00000513787.1:n.821+3A>G
ENST00000344204.9:c.5912+3A>G MANE Select	ENSP00000339299.4:n.5912+3A>G
ENST00000639876.2:c.821+3A>G	ENSP00000492184.2:n.821+3A>G
ENST00000344204.8:c.5912+3A>G	ENSP00000339299.4:n.5912+3A>G
ENST00000512070.6:c.5735+3A>G	ENSP00000421555.2:n.5735+3A>G
ENST00000513206.5:c.5111+3A>G	ENSP00000426342.2:n.5111+3A>G
ENST00000515144.5:n.4830+3A>G
ENST00000620511.1:c.152+3A>G	ENSP00000483869.1:n.152+3A>G
NM_007118.2:c.5912+3A>G	NP_009049.2:n.5912+3A>G
XM_011514107.1:c.5849+3A>G	XP_011512409.1:n.5849+3A>G
XM_011514108.1:c.5795+3A>G	XP_011512410.1:n.5795+3A>G
XM_011514109.1:c.5765+3A>G	XP_011512411.1:n.5765+3A>G
XM_011514110.1:c.5735+3A>G	XP_011512412.1:n.5735+3A>G
XM_011514111.1:c.5735+3A>G	XP_011512413.1:n.5735+3A>G
XM_011514112.1:c.4457+3A>G	XP_011512414.1:n.4457+3A>G
XR_241714.1:n.5930+3A>G
NM_007118.3:c.5912+3A>G	NP_009049.2:n.5912+3A>G
NR_134469.1:n.5936+3A>G
XM_011514107.2:c.5849+3A>G	XP_011512409.1:n.5849+3A>G
XM_011514109.3:c.5765+3A>G	XP_011512411.1:n.5765+3A>G
XM_011514110.3:c.5735+3A>G	XP_011512412.1:n.5735+3A>G
XM_017009801.1:c.5912+3A>G	XP_016865290.1:n.5912+3A>G
XM_017009802.1:c.5912+3A>G	XP_016865291.1:n.5912+3A>G
XM_017009803.1:c.4457+3A>G	XP_016865292.1:n.4457+3A>G
NM_007118.4:c.5912+3A>G MANE Select	NP_009049.2:n.5912+3A>G
NR_134469.2:n.6296+3A>G