Canonical Allele Identifier: CA2695228967
Gene: FTL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48965344C>G , CM000681.2:g.48965344C>G GRCh38
NC_000019.9:g.49468601C>G , CM000681.1:g.49468601C>G GRCh37
NC_000019.8:g.54160413C>G NCBI36
NG_008152.1:g.5036C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331825.11:c.-164C>G MANE Select ENSP00000366525.2:n.-164C>G
ENST00000331825.10:c.-164C>G ENSP00000366525.2:n.-164C>G
ENST00000622577.2:c.-164C>G ENSP00000484043.1:n.-164C>G
NM_000146.3:c.-164C>G NP_000137.2:n.-164C>G
XM_024451447.1:c.347C>G XP_024307215.1:p.Ser116Ter
NM_000146.4:c.-164C>G MANE Select NP_000137.2:n.-164C>G