Canonical Allele Identifier: CA406756757
Gene: FTL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48966323A>C , CM000681.2:g.48966323A>C GRCh38
NC_000019.9:g.49469580A>C , CM000681.1:g.49469580A>C GRCh37
NC_000019.8:g.54161392A>C NCBI36
NG_008152.1:g.6015A>C
NG_012923.1:g.32031T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331825.11:c.292A>C MANE Select ENSP00000366525.2:p.Lys98Gln
ENST00000331825.10:c.292A>C ENSP00000366525.2:p.Lys98Gln
ENST00000622577.2:c.292A>C ENSP00000484043.1:p.Lys98Gln
NM_000146.3:c.292A>C NP_000137.2:p.Lys98Gln
XM_024451447.1:c.802A>C XP_024307215.1:p.Lys268Gln
NM_000146.4:c.292A>C MANE Select NP_000137.2:p.Lys98Gln