Canonical Allele Identifier: CA2340161168

Gene: FTL

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48965347C= , CM000681.2:g.48965347C=	GRCh38
NC_000019.9:g.49468604C= , CM000681.1:g.49468604C=	GRCh37
NC_000019.8:g.54160416C=	NCBI36
NG_008152.1:g.5039C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331825.11:c.-161C= MANE Select	ENSP00000366525.2:n.-161C=
ENST00000331825.10:c.-161C=	ENSP00000366525.2:n.-161C=
ENST00000622577.2:c.-161C=	ENSP00000484043.1:n.-161C=
NM_000146.3:c.-161C=	NP_000137.2:n.-161C=
XM_024451447.1:c.350C=	XP_024307215.1:p.Thr117=
NM_000146.4:c.-161C= MANE Select	NP_000137.2:n.-161C=