Canonical Allele Identifier: CA2340161445

Gene: FTL

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48965765C= , CM000681.2:g.48965765C=	GRCh38
NC_000019.9:g.49469022C= , CM000681.1:g.49469022C=	GRCh37
NC_000019.8:g.54160834C=	NCBI36
NG_008152.1:g.5457C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000331825.11:c.103-5C= MANE Select	ENSP00000366525.2:n.103-5C=
ENST00000331825.10:c.103-5C=	ENSP00000366525.2:n.103-5C=
ENST00000622577.2:c.103-5C=	ENSP00000484043.1:n.103-5C=
NM_000146.3:c.103-5C=	NP_000137.2:n.103-5C=
XM_024451447.1:c.613-5C=	XP_024307215.1:n.613-5C=
NM_000146.4:c.103-5C= MANE Select	NP_000137.2:n.103-5C=