Canonical Allele Identifier: CA406755961

Gene: FTL

Linked Data

• MyVariant Identifiers: chr19:g.49469026G>T (hg19) ; chr19:g.48965769G>T (hg38)

Genomic Alleles

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

Transcript Alleles

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