Canonical Allele Identifier: CA2340161165
Gene: FTL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48965345A= , CM000681.2:g.48965345A= GRCh38
NC_000019.9:g.49468602A= , CM000681.1:g.49468602A= GRCh37
NC_000019.8:g.54160414A= NCBI36
NG_008152.1:g.5037A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331825.11:c.-163A= MANE Select ENSP00000366525.2:n.-163A=
ENST00000331825.10:c.-163A= ENSP00000366525.2:n.-163A=
ENST00000622577.2:c.-163A= ENSP00000484043.1:n.-163A=
NM_000146.3:c.-163A= NP_000137.2:n.-163A=
XM_024451447.1:c.348A= XP_024307215.1:p.Ser116=
NM_000146.4:c.-163A= MANE Select NP_000137.2:n.-163A=