Canonical Allele Identifier: CA2340161672
Gene: FTL HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48966191G= , CM000681.2:g.48966191G= GRCh38
NC_000019.9:g.49469448G= , CM000681.1:g.49469448G= GRCh37
NC_000019.8:g.54161260G= NCBI36
NG_008152.1:g.5883G=
NG_012923.1:g.32163C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331825.11:c.250-90G= MANE Select ENSP00000366525.2:n.250-90G=
ENST00000331825.10:c.250-90G= ENSP00000366525.2:n.250-90G=
ENST00000622577.2:c.250-90G= ENSP00000484043.1:n.250-90G=
NM_000146.3:c.250-90G= NP_000137.2:n.250-90G=
XM_024451447.1:c.760-90G= XP_024307215.1:n.760-90G=
NM_000146.4:c.250-90G= MANE Select NP_000137.2:n.250-90G=
Search 100 bp 5'
Search 100 bp 3'