Canonical Allele Identifier: CA359235184

Gene: TRIO

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14481271C>T , CM000667.2:g.14481271C>T	GRCh38
NC_000005.9:g.14481380C>T , CM000667.1:g.14481380C>T	GRCh37
NC_000005.8:g.14534380C>T	NCBI36
NG_052962.1:g.342570C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698542.1:c.1283C>T	ENSP00000513787.1:p.Thr428Ile
ENST00000344204.9:c.6374C>T MANE Select	ENSP00000339299.4:p.Thr2125Ile
ENST00000639876.2:c.1283C>T	ENSP00000492184.2:p.Thr428Ile
ENST00000344204.8:c.6374C>T	ENSP00000339299.4:p.Thr2125Ile
ENST00000511019.1:n.161C>T
ENST00000512070.6:c.6197C>T	ENSP00000421555.2:p.Thr2066Ile
ENST00000513206.5:c.5573C>T	ENSP00000426342.2:p.Thr1858Ile
ENST00000515144.5:n.5292C>T
ENST00000620511.1:c.614C>T	ENSP00000483869.1:p.Thr205Ile
NM_007118.2:c.6374C>T	NP_009049.2:p.Thr2125Ile
XM_011514107.1:c.6311C>T	XP_011512409.1:p.Thr2104Ile
XM_011514108.1:c.6257C>T	XP_011512410.1:p.Thr2086Ile
XM_011514109.1:c.6227C>T	XP_011512411.1:p.Thr2076Ile
XM_011514110.1:c.6197C>T	XP_011512412.1:p.Thr2066Ile
XM_011514111.1:c.6197C>T	XP_011512413.1:p.Thr2066Ile
XM_011514112.1:c.4919C>T	XP_011512414.1:p.Thr1640Ile
XR_241714.1:n.6392C>T
NM_007118.3:c.6374C>T	NP_009049.2:p.Thr2125Ile
NR_134469.1:n.6398C>T
XM_011514107.2:c.6311C>T	XP_011512409.1:p.Thr2104Ile
XM_011514109.3:c.6227C>T	XP_011512411.1:p.Thr2076Ile
XM_011514110.3:c.6197C>T	XP_011512412.1:p.Thr2066Ile
XM_017009801.1:c.6374C>T	XP_016865290.1:p.Thr2125Ile
XM_017009802.1:c.6374C>T	XP_016865291.1:p.Thr2125Ile
XM_017009803.1:c.4919C>T	XP_016865292.1:p.Thr1640Ile
NM_007118.4:c.6374C>T MANE Select	NP_009049.2:p.Thr2125Ile
NR_134469.2:n.6758C>T