Canonical Allele Identifier: CA2340161596

Gene: FTL

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48966039T= , CM000681.2:g.48966039T=	GRCh38
NC_000019.9:g.49469296T= , CM000681.1:g.49469296T=	GRCh37
NC_000019.8:g.54161108T=	NCBI36
NG_008152.1:g.5731T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331825.11:c.249+123T= MANE Select	ENSP00000366525.2:n.249+123T=
ENST00000331825.10:c.249+123T=	ENSP00000366525.2:n.249+123T=
ENST00000622577.2:c.249+123T=	ENSP00000484043.1:n.249+123T=
NM_000146.3:c.249+123T=	NP_000137.2:n.249+123T=
XM_024451447.1:c.759+123T=	XP_024307215.1:n.759+123T=
NM_000146.4:c.249+123T= MANE Select	NP_000137.2:n.249+123T=