Canonical Allele Identifier: CA2355728

Gene: LTF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46456312C>T , CM000665.2:g.46456312C>T	GRCh38
NC_000003.11:g.46497802C>T , CM000665.1:g.46497802C>T	GRCh37
NC_000003.10:g.46472806C>T	NCBI36
NG_023257.1:g.13594G>A
NG_023257.2:g.33923G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231751.9:c.294G>A MANE Select	ENSP00000231751.4:p.Ala98=
ENST00000231751.8:c.294G>A	ENSP00000231751.4:p.Ala98=
ENST00000417439.5:c.294G>A	ENSP00000405546.1:p.Ala98=
ENST00000426532.6:c.162G>A	ENSP00000405719.2:p.Ala54=
ENST00000431944.1:c.327G>A	ENSP00000395234.1:p.Ala109=
ENST00000443496.5:c.255G>A	ENSP00000397427.1:p.Ala85=
ENST00000478874.2:n.178+7155G>A
NM_001199149.1:c.162G>A	NP_001186078.1:p.Ala54=
NM_002343.4:c.294G>A	NP_002334.2:p.Ala98=
NM_001321121.1:c.294G>A	NP_001308050.1:p.Ala98=
NM_001321122.1:c.255G>A	NP_001308051.1:p.Ala85=
NM_002343.5:c.294G>A	NP_002334.2:p.Ala98=
NM_001199149.2:c.162G>A	NP_001186078.1:p.Ala54=
NM_001321121.2:c.294G>A	NP_001308050.1:p.Ala98=
NM_002343.6:c.294G>A MANE Select	NP_002334.2:p.Ala98=
NM_001321122.2:c.255G>A	NP_001308051.1:p.Ala85=