Canonical Allele Identifier: CA2586288131
Gene: FTL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48965742C>T , CM000681.2:g.48965742C>T GRCh38
NC_000019.9:g.49468999C>T , CM000681.1:g.49468999C>T GRCh37
NC_000019.8:g.54160811C>T NCBI36
NG_008152.1:g.5434C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000331825.11:c.103-28C>T MANE Select ENSP00000366525.2:n.103-28C>T
ENST00000331825.10:c.103-28C>T ENSP00000366525.2:n.103-28C>T
ENST00000622577.2:c.103-28C>T ENSP00000484043.1:n.103-28C>T
NM_000146.3:c.103-28C>T NP_000137.2:n.103-28C>T
XM_024451447.1:c.613-28C>T XP_024307215.1:n.613-28C>T
NM_000146.4:c.103-28C>T MANE Select NP_000137.2:n.103-28C>T