Canonical Allele Identifier: CA2586288289
Gene: FTL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48966108del , CM000681.2:g.48966108del GRCh38
NC_000019.9:g.49469365del , CM000681.1:g.49469365del GRCh37
NC_000019.8:g.54161177del NCBI36
NG_008152.1:g.5800del

Transcript Alleles

HGVS Amino-acid Change
ENST00000331825.11:c.250-173del MANE Select ENSP00000366525.2:n.250-173del
ENST00000331825.10:c.250-173del ENSP00000366525.2:n.250-173del
ENST00000622577.2:c.250-173del ENSP00000484043.1:n.250-173del
NM_000146.3:c.250-173del NP_000137.2:n.250-173del
XM_024451447.1:c.760-173del XP_024307215.1:n.760-173del
NM_000146.4:c.250-173del MANE Select NP_000137.2:n.250-173del