Canonical Allele Identifier: CA2340161433
Gene: FTL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48965738C= , CM000681.2:g.48965738C= GRCh38
NC_000019.9:g.49468995C= , CM000681.1:g.49468995C= GRCh37
NC_000019.8:g.54160807C= NCBI36
NG_008152.1:g.5430C=

Transcript Alleles

HGVS Amino-acid change
ENST00000331825.11:c.103-32C= MANE Select ENSP00000366525.2:n.103-32C=
ENST00000331825.10:c.103-32C= ENSP00000366525.2:n.103-32C=
ENST00000622577.2:c.103-32C= ENSP00000484043.1:n.103-32C=
NM_000146.3:c.103-32C= NP_000137.2:n.103-32C=
XM_024451447.1:c.613-32C= XP_024307215.1:n.613-32C=
NM_000146.4:c.103-32C= MANE Select NP_000137.2:n.103-32C=