Canonical Allele Identifier: CA2695228972
Gene: FTL HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48965347C>A , CM000681.2:g.48965347C>A GRCh38
NC_000019.9:g.49468604C>A , CM000681.1:g.49468604C>A GRCh37
NC_000019.8:g.54160416C>A NCBI36
NG_008152.1:g.5039C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000331825.11:c.-161C>A MANE Select ENSP00000366525.2:n.-161C>A
ENST00000331825.10:c.-161C>A ENSP00000366525.2:n.-161C>A
ENST00000622577.2:c.-161C>A ENSP00000484043.1:n.-161C>A
NM_000146.3:c.-161C>A NP_000137.2:n.-161C>A
XM_024451447.1:c.350C>A XP_024307215.1:p.Thr117Lys
NM_000146.4:c.-161C>A MANE Select NP_000137.2:n.-161C>A
Search 100 bp 5'
Search 100 bp 3'