Canonical Allele Identifier: CA4127249

Gene: LFNG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2526869C>T , CM000669.2:g.2526869C>T	GRCh38
NC_000007.13:g.2566503C>T , CM000669.1:g.2566503C>T	GRCh37
NC_000007.12:g.2533029C>T	NCBI36
NG_008109.2:g.19341C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001040167.2:c.1021C>T MANE Select	NP_001035257.1:p.Arg341Trp
ENST00000222725.10:c.1021C>T MANE Select	ENSP00000222725.5:p.Arg341Trp
NM_001040167.1:c.1021C>T	NP_001035257.1:p.Arg341Trp
NM_001040168.1:c.1021C>T	NP_001035258.1:p.Arg341Trp
NM_001040168.2:c.1021C>T	NP_001035258.1:p.Arg341Trp
NM_001166355.1:c.808C>T	NP_001159827.1:p.Arg270Trp
NM_001166355.2:c.808C>T	NP_001159827.1:p.Arg270Trp
NM_002304.2:c.634C>T	NP_002295.1:p.Arg212Trp
NM_002304.3:c.634C>T	NP_002295.1:p.Arg212Trp
ENST00000222725.9:c.1021C>T	ENSP00000222725.5:p.Arg341Trp
ENST00000338732.7:c.634C>T	ENSP00000343095.3:p.Arg212Trp
ENST00000359574.7:c.1021C>T	ENSP00000352579.3:p.Arg341Trp
ENST00000402045.5:c.634C>T	ENSP00000384786.1:p.Arg212Trp
ENST00000402506.5:c.808C>T	ENSP00000385764.1:p.Arg270Trp
ENST00000493850.1:n.802C>T
ENST00000614382.1:c.628C>T	ENSP00000483986.1:p.Arg210Trp