Canonical Allele Identifier: CA113939637

Gene: TRIO

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14271022T>C , CM000667.2:g.14271022T>C	GRCh38
NC_000005.9:g.14271131T>C , CM000667.1:g.14271131T>C	GRCh37
NC_000005.8:g.14324131T>C	NCBI36
NG_052962.1:g.132321T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698541.1:c.232+123T>C	ENSP00000513786.1:n.232+123T>C
ENST00000704488.1:c.103+123T>C	ENSP00000515916.1:n.103+123T>C
ENST00000344204.9:c.232+123T>C MANE Select	ENSP00000339299.4:n.232+123T>C
ENST00000344204.8:c.232+123T>C	ENSP00000339299.4:n.232+123T>C
ENST00000502816.1:n.256+123T>C
ENST00000505971.5:n.256+123T>C
ENST00000509967.6:c.85+123T>C	ENSP00000445592.1:n.85+123T>C
ENST00000512070.6:c.55+123T>C	ENSP00000421555.2:n.55+123T>C
NM_007118.2:c.232+123T>C	NP_009049.2:n.232+123T>C
XM_011514107.1:c.169+123T>C	XP_011512409.1:n.169+123T>C
XM_011514108.1:c.115+123T>C	XP_011512410.1:n.115+123T>C
XM_011514109.1:c.85+123T>C	XP_011512411.1:n.85+123T>C
XM_011514110.1:c.55+123T>C	XP_011512412.1:n.55+123T>C
XM_011514111.1:c.55+123T>C	XP_011512413.1:n.55+123T>C
XM_011514113.1:c.232+123T>C	XP_011512415.1:n.232+123T>C
XR_241714.1:n.250+123T>C
NM_007118.3:c.232+123T>C	NP_009049.2:n.232+123T>C
NR_134469.1:n.256+123T>C
XM_011514107.2:c.169+123T>C	XP_011512409.1:n.169+123T>C
XM_011514109.3:c.85+123T>C	XP_011512411.1:n.85+123T>C
XM_011514110.3:c.55+123T>C	XP_011512412.1:n.55+123T>C
XM_017009801.1:c.232+123T>C	XP_016865290.1:n.232+123T>C
XM_017009802.1:c.232+123T>C	XP_016865291.1:n.232+123T>C
XR_001742236.2:n.608+123T>C
NM_007118.4:c.232+123T>C MANE Select	NP_009049.2:n.232+123T>C
NR_134469.2:n.616+123T>C