Canonical Allele Identifier: CA2586287958
Gene: FTL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48965316G>T , CM000681.2:g.48965316G>T GRCh38
NC_000019.9:g.49468573G>T , CM000681.1:g.49468573G>T GRCh37
NC_000019.8:g.54160385G>T NCBI36
NG_008152.1:g.5008G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000331825.11:c.-192G>T MANE Select ENSP00000366525.2:n.-192G>T
ENST00000331825.10:c.-192G>T ENSP00000366525.2:n.-192G>T
ENST00000622577.2:c.-192G>T ENSP00000484043.1:n.-192G>T
NM_000146.3:c.-192G>T NP_000137.2:n.-192G>T
XM_024451447.1:c.319G>T XP_024307215.1:p.Gly107Cys
NM_000146.4:c.-192G>T MANE Select NP_000137.2:n.-192G>T