Canonical Allele Identifier: CA406756365
Gene: FTL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48965852G>T , CM000681.2:g.48965852G>T GRCh38
NC_000019.9:g.49469109G>T , CM000681.1:g.49469109G>T GRCh37
NC_000019.8:g.54160921G>T NCBI36
NG_008152.1:g.5544G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000331825.11:c.185G>T MANE Select ENSP00000366525.2:p.Gly62Val
ENST00000331825.10:c.185G>T ENSP00000366525.2:p.Gly62Val
ENST00000622577.2:c.185G>T ENSP00000484043.1:p.Gly62Val
NM_000146.3:c.185G>T NP_000137.2:p.Gly62Val
XM_024451447.1:c.695G>T XP_024307215.1:p.Gly232Val
NM_000146.4:c.185G>T MANE Select NP_000137.2:p.Gly62Val