Canonical Allele Identifier: CA366615835

Gene: LFNG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2524696C>T , CM000669.2:g.2524696C>T	GRCh38
NC_000007.13:g.2564330C>T , CM000669.1:g.2564330C>T	GRCh37
NC_000007.12:g.2530856C>T	NCBI36
NG_008109.2:g.17168C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001040167.2:c.434C>T MANE Select	NP_001035257.1:p.Thr145Met
ENST00000222725.10:c.434C>T MANE Select	ENSP00000222725.5:p.Thr145Met
NM_001040167.1:c.434C>T	NP_001035257.1:p.Thr145Met
NM_001040168.1:c.434C>T	NP_001035258.1:p.Thr145Met
NM_001040168.2:c.434C>T	NP_001035258.1:p.Thr145Met
NM_001166355.1:c.221C>T	NP_001159827.1:p.Thr74Met
NM_001166355.2:c.221C>T	NP_001159827.1:p.Thr74Met
NM_002304.2:c.47C>T	NP_002295.1:p.Thr16Met
NM_002304.3:c.47C>T	NP_002295.1:p.Thr16Met
ENST00000222725.9:c.434C>T	ENSP00000222725.5:p.Thr145Met
ENST00000338732.7:c.47C>T	ENSP00000343095.3:p.Thr16Met
ENST00000359574.7:c.434C>T	ENSP00000352579.3:p.Thr145Met
ENST00000402045.5:c.47C>T	ENSP00000384786.1:p.Thr16Met
ENST00000402506.5:c.221C>T	ENSP00000385764.1:p.Thr74Met
ENST00000493850.1:n.120C>T
ENST00000614382.1:c.41C>T	ENSP00000483986.1:p.Thr14Met