Canonical Allele Identifier: CA4127261

Gene: LFNG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2526884G>C , CM000669.2:g.2526884G>C	GRCh38
NC_000007.13:g.2566518G>C , CM000669.1:g.2566518G>C	GRCh37
NC_000007.12:g.2533044G>C	NCBI36
NG_008109.2:g.19356G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222725.10:c.1036G>C MANE Select	ENSP00000222725.5:p.Val346Leu
ENST00000222725.9:c.1036G>C	ENSP00000222725.5:p.Val346Leu
ENST00000338732.7:c.649G>C	ENSP00000343095.3:p.Val217Leu
ENST00000359574.7:c.1036G>C	ENSP00000352579.3:p.Val346Leu
ENST00000402045.5:c.649G>C	ENSP00000384786.1:p.Val217Leu
ENST00000402506.5:c.823G>C	ENSP00000385764.1:p.Val275Leu
ENST00000614382.1:c.643G>C	ENSP00000483986.1:p.Val215Leu
NM_001040167.1:c.1036G>C	NP_001035257.1:p.Val346Leu
NM_001040168.1:c.1036G>C	NP_001035258.1:p.Val346Leu
NM_001166355.1:c.823G>C	NP_001159827.1:p.Val275Leu
NM_002304.2:c.649G>C	NP_002295.1:p.Val217Leu
NM_001040167.2:c.1036G>C MANE Select	NP_001035257.1:p.Val346Leu
NM_001040168.2:c.1036G>C	NP_001035258.1:p.Val346Leu
NM_001166355.2:c.823G>C	NP_001159827.1:p.Val275Leu
NM_002304.3:c.649G>C	NP_002295.1:p.Val217Leu