Canonical Allele Identifier: CA2576844638
Gene: FTL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48965762T>C , CM000681.2:g.48965762T>C GRCh38
NC_000019.9:g.49469019T>C , CM000681.1:g.49469019T>C GRCh37
NC_000019.8:g.54160831T>C NCBI36
NG_008152.1:g.5454T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000331825.11:c.103-8T>C MANE Select ENSP00000366525.2:n.103-8T>C
ENST00000331825.10:c.103-8T>C ENSP00000366525.2:n.103-8T>C
ENST00000622577.2:c.103-8T>C ENSP00000484043.1:n.103-8T>C
NM_000146.3:c.103-8T>C NP_000137.2:n.103-8T>C
XM_024451447.1:c.613-8T>C XP_024307215.1:n.613-8T>C
NM_000146.4:c.103-8T>C MANE Select NP_000137.2:n.103-8T>C
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