Canonical Allele Identifier: CA2340161649

Gene: FTL

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48966129A= , CM000681.2:g.48966129A=	GRCh38
NC_000019.9:g.49469386A= , CM000681.1:g.49469386A=	GRCh37
NC_000019.8:g.54161198A=	NCBI36
NG_008152.1:g.5821A=
NG_012923.1:g.32225T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331825.11:c.250-152A= MANE Select	ENSP00000366525.2:n.250-152A=
ENST00000331825.10:c.250-152A=	ENSP00000366525.2:n.250-152A=
ENST00000622577.2:c.250-152A=	ENSP00000484043.1:n.250-152A=
NM_000146.3:c.250-152A=	NP_000137.2:n.250-152A=
XM_024451447.1:c.760-152A=	XP_024307215.1:n.760-152A=
NM_000146.4:c.250-152A= MANE Select	NP_000137.2:n.250-152A=