Canonical Allele Identifier: CA2814670109
Gene: FTL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48966162dup , CM000681.2:g.48966162dup GRCh38
NC_000019.9:g.49469419dup , CM000681.1:g.49469419dup GRCh37
NC_000019.8:g.54161231dup NCBI36
NG_008152.1:g.5854dup
NG_012923.1:g.32192dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000331825.11:c.250-119dup MANE Select ENSP00000366525.2:n.250-119dup
ENST00000331825.10:c.250-119dup ENSP00000366525.2:n.250-119dup
ENST00000622577.2:c.250-119dup ENSP00000484043.1:n.250-119dup
NM_000146.3:c.250-119dup NP_000137.2:n.250-119dup
XM_024451447.1:c.760-119dup XP_024307215.1:n.760-119dup
NM_000146.4:c.250-119dup MANE Select NP_000137.2:n.250-119dup