Canonical Allele Identifier: CA2340161449

Gene: FTL

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48965769G= , CM000681.2:g.48965769G=	GRCh38
NC_000019.9:g.49469026G= , CM000681.1:g.49469026G=	GRCh37
NC_000019.8:g.54160838G=	NCBI36
NG_008152.1:g.5461G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331825.11:c.103-1G= MANE Select	ENSP00000366525.2:n.103-1G=
ENST00000331825.10:c.103-1G=	ENSP00000366525.2:n.103-1G=
ENST00000622577.2:c.103-1G=	ENSP00000484043.1:n.103-1G=
NM_000146.3:c.103-1G=	NP_000137.2:n.103-1G=
XM_024451447.1:c.613-1G=	XP_024307215.1:n.613-1G=
NM_000146.4:c.103-1G= MANE Select	NP_000137.2:n.103-1G=