Canonical Allele Identifier: CA2340161437
Gene: FTL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48965746T= , CM000681.2:g.48965746T= GRCh38
NC_000019.9:g.49469003T= , CM000681.1:g.49469003T= GRCh37
NC_000019.8:g.54160815T= NCBI36
NG_008152.1:g.5438T=

Transcript Alleles

HGVS Amino-acid change
ENST00000331825.11:c.103-24T= MANE Select ENSP00000366525.2:n.103-24T=
ENST00000331825.10:c.103-24T= ENSP00000366525.2:n.103-24T=
ENST00000622577.2:c.103-24T= ENSP00000484043.1:n.103-24T=
NM_000146.3:c.103-24T= NP_000137.2:n.103-24T=
XM_024451447.1:c.613-24T= XP_024307215.1:n.613-24T=
NM_000146.4:c.103-24T= MANE Select NP_000137.2:n.103-24T=