Canonical Allele Identifier: CA4126912

Gene: LFNG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2520188G>T , CM000669.2:g.2520188G>T	GRCh38
NC_000007.13:g.2559822G>T , CM000669.1:g.2559822G>T	GRCh37
NC_000007.12:g.2526348G>T	NCBI36
NG_008109.2:g.12660G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001040167.2:c.327G>T MANE Select	NP_001035257.1:p.Pro109=
ENST00000222725.10:c.327G>T MANE Select	ENSP00000222725.5:p.Pro109=
NM_001040167.1:c.327G>T	NP_001035257.1:p.Pro109=
NM_001040168.1:c.327G>T	NP_001035258.1:p.Pro109=
NM_001040168.2:c.327G>T	NP_001035258.1:p.Pro109=
NM_001166355.1:c.220-4507G>T	NP_001159827.1:n.220-4507G>T
NM_001166355.2:c.220-4507G>T	NP_001159827.1:n.220-4507G>T
NM_002304.2:c.45+1590G>T	NP_002295.1:n.45+1590G>T
NM_002304.3:c.45+1590G>T	NP_002295.1:n.45+1590G>T
ENST00000222725.9:c.327G>T	ENSP00000222725.5:p.Pro109=
ENST00000338732.7:c.45+1590G>T	ENSP00000343095.3:n.45+1590G>T
ENST00000359574.7:c.327G>T	ENSP00000352579.3:p.Pro109=
ENST00000402045.5:c.45+1590G>T	ENSP00000384786.1:n.45+1590G>T
ENST00000402506.5:c.220-4507G>T	ENSP00000385764.1:n.220-4507G>T