Canonical Allele Identifier: CA2340161622
Gene: FTL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48966085G= , CM000681.2:g.48966085G= GRCh38
NC_000019.9:g.49469342G= , CM000681.1:g.49469342G= GRCh37
NC_000019.8:g.54161154G= NCBI36
NG_008152.1:g.5777G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331825.11:c.249+169G= MANE Select ENSP00000366525.2:n.249+169G=
ENST00000331825.10:c.249+169G= ENSP00000366525.2:n.249+169G=
ENST00000622577.2:c.249+169G= ENSP00000484043.1:n.249+169G=
NM_000146.3:c.249+169G= NP_000137.2:n.249+169G=
XM_024451447.1:c.759+169G= XP_024307215.1:n.759+169G=
NM_000146.4:c.249+169G= MANE Select NP_000137.2:n.249+169G=
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