Canonical Allele Identifier: CA406756851
Gene: FTL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48966348A>G , CM000681.2:g.48966348A>G GRCh38
NC_000019.9:g.49469605A>G , CM000681.1:g.49469605A>G GRCh37
NC_000019.8:g.54161417A>G NCBI36
NG_008152.1:g.6040A>G
NG_012923.1:g.32006T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000331825.11:c.317A>G MANE Select ENSP00000366525.2:p.Lys106Arg
ENST00000331825.10:c.317A>G ENSP00000366525.2:p.Lys106Arg
ENST00000622577.2:c.317A>G ENSP00000484043.1:p.Lys106Arg
NM_000146.3:c.317A>G NP_000137.2:p.Lys106Arg
XM_024451447.1:c.827A>G XP_024307215.1:p.Lys276Arg
NM_000146.4:c.317A>G MANE Select NP_000137.2:p.Lys106Arg