Canonical Allele Identifier: CA2340161150

Gene: FTL

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48965325G= , CM000681.2:g.48965325G=	GRCh38
NC_000019.9:g.49468582G= , CM000681.1:g.49468582G=	GRCh37
NC_000019.8:g.54160394G=	NCBI36
NG_008152.1:g.5017G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331825.11:c.-183G= MANE Select	ENSP00000366525.2:n.-183G=
ENST00000331825.10:c.-183G=	ENSP00000366525.2:n.-183G=
ENST00000622577.2:c.-183G=	ENSP00000484043.1:n.-183G=
NM_000146.3:c.-183G=	NP_000137.2:n.-183G=
XM_024451447.1:c.328G=	XP_024307215.1:p.Ala110=
NM_000146.4:c.-183G= MANE Select	NP_000137.2:n.-183G=