Canonical Allele Identifier: CA359283267

Gene: TRIO

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14143802C>A , CM000667.2:g.14143802C>A	GRCh38
NC_000005.9:g.14143911C>A , CM000667.1:g.14143911C>A	GRCh37
NC_000005.8:g.14196911C>A	NCBI36
NG_052962.1:g.5101C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_007118.4:c.77C>A MANE Select	NP_009049.2:p.Ser26Ter
ENST00000344204.9:c.77C>A MANE Select	ENSP00000339299.4:p.Ser26Ter
NM_007118.2:c.77C>A	NP_009049.2:p.Ser26Ter
NM_007118.3:c.77C>A	NP_009049.2:p.Ser26Ter
NR_134469.1:n.101C>A
NR_134469.2:n.461C>A
ENST00000344204.8:c.77C>A	ENSP00000339299.4:p.Ser26Ter
ENST00000502816.1:n.101C>A
ENST00000505971.5:n.101C>A
ENST00000698541.1:c.77C>A	ENSP00000513786.1:p.Ser26Ter
XM_011514113.1:c.77C>A	XP_011512415.1:p.Ser26Ter
XM_017009801.1:c.77C>A	XP_016865290.1:p.Ser26Ter
XM_017009802.1:c.77C>A	XP_016865291.1:p.Ser26Ter
XR_001742236.2:n.453C>A
XR_241714.1:n.95C>A