Canonical Allele Identifier: CA406755964
Gene: FTL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48965770G>T , CM000681.2:g.48965770G>T GRCh38
NC_000019.9:g.49469027G>T , CM000681.1:g.49469027G>T GRCh37
NC_000019.8:g.54160839G>T NCBI36
NG_008152.1:g.5462G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000331825.11:c.103G>T MANE Select ENSP00000366525.2:p.Gly35Cys
ENST00000331825.10:c.103G>T ENSP00000366525.2:p.Gly35Cys
ENST00000622577.2:c.103G>T ENSP00000484043.1:p.Gly35Cys
NM_000146.3:c.103G>T NP_000137.2:p.Gly35Cys
XM_024451447.1:c.613G>T XP_024307215.1:p.Gly205Cys
NM_000146.4:c.103G>T MANE Select NP_000137.2:p.Gly35Cys