Canonical Allele Identifier: CA367098491

Gene: TRIL

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.28956083G>A , CM000669.2:g.28956083G>A	GRCh38
NC_000007.13:g.28995699G>A , CM000669.1:g.28995699G>A	GRCh37
NC_000007.12:g.28962224G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539664.3:c.1964C>T MANE Select	ENSP00000479256.1:p.Thr655Ile
ENST00000539664.2:c.1964C>T	ENSP00000479256.1:p.Thr655Ile
NM_014817.3:c.1964C>T	NP_055632.2:p.Thr655Ile
NM_014817.4:c.1964C>T MANE Select	NP_055632.2:p.Thr655Ile