Canonical Allele Identifier: CA2340161610
Gene: FTL HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48966066C= , CM000681.2:g.48966066C= GRCh38
NC_000019.9:g.49469323C= , CM000681.1:g.49469323C= GRCh37
NC_000019.8:g.54161135C= NCBI36
NG_008152.1:g.5758C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331825.11:c.249+150C= MANE Select ENSP00000366525.2:n.249+150C=
ENST00000331825.10:c.249+150C= ENSP00000366525.2:n.249+150C=
ENST00000622577.2:c.249+150C= ENSP00000484043.1:n.249+150C=
NM_000146.3:c.249+150C= NP_000137.2:n.249+150C=
XM_024451447.1:c.759+150C= XP_024307215.1:n.759+150C=
NM_000146.4:c.249+150C= MANE Select NP_000137.2:n.249+150C=
Search 100 bp 5'
Search 100 bp 3'