Canonical Allele Identifier: CA406756346

Gene: FTL

Linked Data

• MyVariant Identifiers: chr19:g.49469106A>G (hg19) ; chr19:g.48965849A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48965849A>G , CM000681.2:g.48965849A>G	GRCh38
NC_000019.9:g.49469106A>G , CM000681.1:g.49469106A>G	GRCh37
NC_000019.8:g.54160918A>G	NCBI36
NG_008152.1:g.5541A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000331825.11:c.182A>G MANE Select	ENSP00000366525.2:p.Glu61Gly
ENST00000331825.10:c.182A>G	ENSP00000366525.2:p.Glu61Gly
ENST00000622577.2:c.182A>G	ENSP00000484043.1:p.Glu61Gly
NM_000146.3:c.182A>G	NP_000137.2:p.Glu61Gly
XM_024451447.1:c.692A>G	XP_024307215.1:p.Glu231Gly
NM_000146.4:c.182A>G MANE Select	NP_000137.2:p.Glu61Gly