Canonical Allele Identifier: CA2340161609
Gene: FTL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48966064C= , CM000681.2:g.48966064C= GRCh38
NC_000019.9:g.49469321C= , CM000681.1:g.49469321C= GRCh37
NC_000019.8:g.54161133C= NCBI36
NG_008152.1:g.5756C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331825.11:c.249+148C= MANE Select ENSP00000366525.2:n.249+148C=
ENST00000331825.10:c.249+148C= ENSP00000366525.2:n.249+148C=
ENST00000622577.2:c.249+148C= ENSP00000484043.1:n.249+148C=
NM_000146.3:c.249+148C= NP_000137.2:n.249+148C=
XM_024451447.1:c.759+148C= XP_024307215.1:n.759+148C=
NM_000146.4:c.249+148C= MANE Select NP_000137.2:n.249+148C=
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