Canonical Allele Identifier: CA2340161441
Gene: FTL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48965754C= , CM000681.2:g.48965754C= GRCh38
NC_000019.9:g.49469011C= , CM000681.1:g.49469011C= GRCh37
NC_000019.8:g.54160823C= NCBI36
NG_008152.1:g.5446C=

Transcript Alleles

HGVS Amino-acid change
ENST00000331825.11:c.103-16C= MANE Select ENSP00000366525.2:n.103-16C=
ENST00000331825.10:c.103-16C= ENSP00000366525.2:n.103-16C=
ENST00000622577.2:c.103-16C= ENSP00000484043.1:n.103-16C=
NM_000146.3:c.103-16C= NP_000137.2:n.103-16C=
XM_024451447.1:c.613-16C= XP_024307215.1:n.613-16C=
NM_000146.4:c.103-16C= MANE Select NP_000137.2:n.103-16C=