Canonical Allele Identifier: CA366617384

Gene: LFNG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2525433G>A , CM000669.2:g.2525433G>A	GRCh38
NC_000007.13:g.2565067G>A , CM000669.1:g.2565067G>A	GRCh37
NC_000007.12:g.2531593G>A	NCBI36
NG_008109.2:g.17905G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001040167.2:c.601G>A MANE Select	NP_001035257.1:p.Asp201Asn
ENST00000222725.10:c.601G>A MANE Select	ENSP00000222725.5:p.Asp201Asn
NM_001040167.1:c.601G>A	NP_001035257.1:p.Asp201Asn
NM_001040168.1:c.601G>A	NP_001035258.1:p.Asp201Asn
NM_001040168.2:c.601G>A	NP_001035258.1:p.Asp201Asn
NM_001166355.1:c.388G>A	NP_001159827.1:p.Asp130Asn
NM_001166355.2:c.388G>A	NP_001159827.1:p.Asp130Asn
NM_002304.2:c.214G>A	NP_002295.1:p.Asp72Asn
NM_002304.3:c.214G>A	NP_002295.1:p.Asp72Asn
ENST00000222725.9:c.601G>A	ENSP00000222725.5:p.Asp201Asn
ENST00000338732.7:c.214G>A	ENSP00000343095.3:p.Asp72Asn
ENST00000359574.7:c.601G>A	ENSP00000352579.3:p.Asp201Asn
ENST00000402045.5:c.214G>A	ENSP00000384786.1:p.Asp72Asn
ENST00000402506.5:c.388G>A	ENSP00000385764.1:p.Asp130Asn
ENST00000493850.1:n.382G>A
ENST00000614382.1:c.208G>A	ENSP00000483986.1:p.Asp70Asn