Canonical Allele Identifier: CA113991900

Gene: TRIO

Linked Data

• dbSNP Id: rs571085328
• gnomAD v2: 5-14393581-C-G
• gnomAD v3: 5-14393472-C-G
• gnomAD v4: 5-14393472-C-G
• MyVariant Identifiers: chr5:g.14393581C>G (hg19) ; chr5:g.14393472C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14393472C>G , CM000667.2:g.14393472C>G	GRCh38
NC_000005.9:g.14393581C>G , CM000667.1:g.14393581C>G	GRCh37
NC_000005.8:g.14446581C>G	NCBI36
NG_052962.1:g.254771C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698541.1:c.4219-566C>G	ENSP00000513786.1:n.4219-566C>G
ENST00000344204.9:c.4219-566C>G MANE Select	ENSP00000339299.4:n.4219-566C>G
ENST00000344204.8:c.4219-566C>G	ENSP00000339299.4:n.4219-566C>G
ENST00000502490.1:n.407-566C>G
ENST00000509967.6:c.4072-566C>G	ENSP00000445592.1:n.4072-566C>G
ENST00000512070.6:c.4042-566C>G	ENSP00000421555.2:n.4042-566C>G
ENST00000513206.5:c.3418-566C>G	ENSP00000426342.2:n.3418-566C>G
ENST00000515144.5:n.3137-566C>G
NM_007118.2:c.4219-566C>G	NP_009049.2:n.4219-566C>G
XM_011514107.1:c.4156-566C>G	XP_011512409.1:n.4156-566C>G
XM_011514108.1:c.4102-566C>G	XP_011512410.1:n.4102-566C>G
XM_011514109.1:c.4072-566C>G	XP_011512411.1:n.4072-566C>G
XM_011514110.1:c.4042-566C>G	XP_011512412.1:n.4042-566C>G
XM_011514111.1:c.4042-566C>G	XP_011512413.1:n.4042-566C>G
XM_011514112.1:c.2764-566C>G	XP_011512414.1:n.2764-566C>G
XM_011514113.1:c.4219-566C>G	XP_011512415.1:n.4219-566C>G
XR_241714.1:n.4237-566C>G
NM_007118.3:c.4219-566C>G	NP_009049.2:n.4219-566C>G
NR_134469.1:n.4243-566C>G
XM_011514107.2:c.4156-566C>G	XP_011512409.1:n.4156-566C>G
XM_011514109.3:c.4072-566C>G	XP_011512411.1:n.4072-566C>G
XM_011514110.3:c.4042-566C>G	XP_011512412.1:n.4042-566C>G
XM_017009801.1:c.4219-566C>G	XP_016865290.1:n.4219-566C>G
XM_017009802.1:c.4219-566C>G	XP_016865291.1:n.4219-566C>G
XM_017009803.1:c.2764-566C>G	XP_016865292.1:n.2764-566C>G
XR_001742236.2:n.4595-566C>G
NM_007118.4:c.4219-566C>G MANE Select	NP_009049.2:n.4219-566C>G
NR_134469.2:n.4603-566C>G