Canonical Allele Identifier: CA4126919

Gene: LFNG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2520229A>G , CM000669.2:g.2520229A>G	GRCh38
NC_000007.13:g.2559863A>G , CM000669.1:g.2559863A>G	GRCh37
NC_000007.12:g.2526389A>G	NCBI36
NG_008109.2:g.12701A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001040167.2:c.368A>G MANE Select	NP_001035257.1:p.Lys123Arg
ENST00000222725.10:c.368A>G MANE Select	ENSP00000222725.5:p.Lys123Arg
NM_001040167.1:c.368A>G	NP_001035257.1:p.Lys123Arg
NM_001040168.1:c.368A>G	NP_001035258.1:p.Lys123Arg
NM_001040168.2:c.368A>G	NP_001035258.1:p.Lys123Arg
NM_001166355.1:c.220-4466A>G	NP_001159827.1:n.220-4466A>G
NM_001166355.2:c.220-4466A>G	NP_001159827.1:n.220-4466A>G
NM_002304.2:c.45+1631A>G	NP_002295.1:n.45+1631A>G
NM_002304.3:c.45+1631A>G	NP_002295.1:n.45+1631A>G
ENST00000222725.9:c.368A>G	ENSP00000222725.5:p.Lys123Arg
ENST00000338732.7:c.45+1631A>G	ENSP00000343095.3:n.45+1631A>G
ENST00000359574.7:c.368A>G	ENSP00000352579.3:p.Lys123Arg
ENST00000402045.5:c.45+1631A>G	ENSP00000384786.1:n.45+1631A>G
ENST00000402506.5:c.220-4466A>G	ENSP00000385764.1:n.220-4466A>G