Canonical Allele Identifier: CA73703507

Gene: LTF

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46439310A>T , CM000665.2:g.46439310A>T	GRCh38
NC_000003.11:g.46480801A>T , CM000665.1:g.46480801A>T	GRCh37
NC_000003.10:g.46455805A>T	NCBI36
NG_023257.1:g.30595T>A
NG_023257.2:g.50925T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231751.9:c.1894T>A MANE Select	ENSP00000231751.4:p.Leu632Met
ENST00000231751.8:c.1894T>A	ENSP00000231751.4:p.Leu632Met
ENST00000417439.5:c.1888T>A	ENSP00000405546.1:p.Leu630Met
ENST00000426532.6:c.1762T>A	ENSP00000405719.2:p.Leu588Met
ENST00000443496.5:c.1855T>A	ENSP00000397427.1:p.Leu619Met
ENST00000478874.2:n.417T>A
ENST00000493056.5:n.383T>A
NM_001199149.1:c.1762T>A	NP_001186078.1:p.Leu588Met
NM_002343.4:c.1894T>A	NP_002334.2:p.Leu632Met
NM_001321121.1:c.1888T>A	NP_001308050.1:p.Leu630Met
NM_001321122.1:c.1855T>A	NP_001308051.1:p.Leu619Met
NM_002343.5:c.1894T>A	NP_002334.2:p.Leu632Met
NM_001199149.2:c.1762T>A	NP_001186078.1:p.Leu588Met
NM_001321121.2:c.1888T>A	NP_001308050.1:p.Leu630Met
NM_002343.6:c.1894T>A MANE Select	NP_002334.2:p.Leu632Met
NM_001321122.2:c.1855T>A	NP_001308051.1:p.Leu619Met