Canonical Allele Identifier: CA352476311

Gene: LTF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46448915C>A , CM000665.2:g.46448915C>A	GRCh38
NC_000003.11:g.46490406C>A , CM000665.1:g.46490406C>A	GRCh37
NC_000003.10:g.46465410C>A	NCBI36
NG_023257.1:g.20990G>T
NG_023257.2:g.41320G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231751.9:c.1160G>T MANE Select	ENSP00000231751.4:p.Ser387Ile
ENST00000231751.8:c.1160G>T	ENSP00000231751.4:p.Ser387Ile
ENST00000417439.5:c.1160G>T	ENSP00000405546.1:p.Ser387Ile
ENST00000426532.6:c.1028G>T	ENSP00000405719.2:p.Ser343Ile
ENST00000443496.5:c.1121G>T	ENSP00000397427.1:p.Ser374Ile
ENST00000478874.2:n.179-7432G>T
NM_001199149.1:c.1028G>T	NP_001186078.1:p.Ser343Ile
NM_002343.4:c.1160G>T	NP_002334.2:p.Ser387Ile
NM_001321121.1:c.1160G>T	NP_001308050.1:p.Ser387Ile
NM_001321122.1:c.1121G>T	NP_001308051.1:p.Ser374Ile
NM_002343.5:c.1160G>T	NP_002334.2:p.Ser387Ile
NM_001199149.2:c.1028G>T	NP_001186078.1:p.Ser343Ile
NM_001321121.2:c.1160G>T	NP_001308050.1:p.Ser387Ile
NM_002343.6:c.1160G>T MANE Select	NP_002334.2:p.Ser387Ile
NM_001321122.2:c.1121G>T	NP_001308051.1:p.Ser374Ile