Canonical Allele Identifier: CA114683590

Gene: TRIO

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14143769C>T , CM000667.2:g.14143769C>T	GRCh38
NC_000005.9:g.14143878C>T , CM000667.1:g.14143878C>T	GRCh37
NC_000005.8:g.14196878C>T	NCBI36
NG_052962.1:g.5068C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_007118.4:c.44C>T MANE Select	NP_009049.2:p.Ser15Phe
ENST00000344204.9:c.44C>T MANE Select	ENSP00000339299.4:p.Ser15Phe
NM_007118.2:c.44C>T	NP_009049.2:p.Ser15Phe
NM_007118.3:c.44C>T	NP_009049.2:p.Ser15Phe
NR_134469.1:n.68C>T
NR_134469.2:n.428C>T
ENST00000344204.8:c.44C>T	ENSP00000339299.4:p.Ser15Phe
ENST00000502816.1:n.68C>T
ENST00000505971.5:n.68C>T
ENST00000698541.1:c.44C>T	ENSP00000513786.1:p.Ser15Phe
XM_011514113.1:c.44C>T	XP_011512415.1:p.Ser15Phe
XM_017009801.1:c.44C>T	XP_016865290.1:p.Ser15Phe
XM_017009802.1:c.44C>T	XP_016865291.1:p.Ser15Phe
XR_001742236.2:n.420C>T
XR_241714.1:n.62C>T