Canonical Allele Identifier: CA126552

Gene: FTL

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48965340G>A , CM000681.2:g.48965340G>A	GRCh38
NC_000019.9:g.49468597G>A , CM000681.1:g.49468597G>A	GRCh37
NC_000019.8:g.54160409G>A	NCBI36
NG_008152.1:g.5032G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331825.11:c.-168G>A MANE Select	ENSP00000366525.2:n.-168G>A
ENST00000331825.10:c.-168G>A	ENSP00000366525.2:n.-168G>A
ENST00000622577.2:c.-168G>A	ENSP00000484043.1:n.-168G>A
NM_000146.3:c.-168G>A	NP_000137.2:n.-168G>A
XM_024451447.1:c.343G>A	XP_024307215.1:p.Ala115Thr
NM_000146.4:c.-168G>A MANE Select	NP_000137.2:n.-168G>A