Canonical Allele Identifier: CA2586288258
Gene: FTL HGNC NCBI

Linked Data

gnomAD v4: 19-48966081-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48966081A>G , CM000681.2:g.48966081A>G GRCh38
NC_000019.9:g.49469338A>G , CM000681.1:g.49469338A>G GRCh37
NC_000019.8:g.54161150A>G NCBI36
NG_008152.1:g.5773A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331825.11:c.249+165A>G MANE Select ENSP00000366525.2:n.249+165A>G
ENST00000331825.10:c.249+165A>G ENSP00000366525.2:n.249+165A>G
ENST00000622577.2:c.249+165A>G ENSP00000484043.1:n.249+165A>G
NM_000146.3:c.249+165A>G NP_000137.2:n.249+165A>G
XM_024451447.1:c.759+165A>G XP_024307215.1:n.759+165A>G
NM_000146.4:c.249+165A>G MANE Select NP_000137.2:n.249+165A>G
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