Canonical Allele Identifier: CA366617018

Gene: LFNG

Linked Data

• MyVariant Identifiers: chr7:g.2564933T>C (hg19) ; chr7:g.2525299T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2525299T>C , CM000669.2:g.2525299T>C	GRCh38
NC_000007.13:g.2564933T>C , CM000669.1:g.2564933T>C	GRCh37
NC_000007.12:g.2531459T>C	NCBI36
NG_008109.2:g.17771T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222725.10:c.562T>C MANE Select	ENSP00000222725.5:p.Phe188Leu
ENST00000222725.9:c.562T>C	ENSP00000222725.5:p.Phe188Leu
ENST00000338732.7:c.175T>C	ENSP00000343095.3:p.Phe59Leu
ENST00000359574.7:c.562T>C	ENSP00000352579.3:p.Phe188Leu
ENST00000402045.5:c.175T>C	ENSP00000384786.1:p.Phe59Leu
ENST00000402506.5:c.349T>C	ENSP00000385764.1:p.Phe117Leu
ENST00000493850.1:n.248T>C
ENST00000614382.1:c.169T>C	ENSP00000483986.1:p.Phe57Leu
NM_001040167.1:c.562T>C	NP_001035257.1:p.Phe188Leu
NM_001040168.1:c.562T>C	NP_001035258.1:p.Phe188Leu
NM_001166355.1:c.349T>C	NP_001159827.1:p.Phe117Leu
NM_002304.2:c.175T>C	NP_002295.1:p.Phe59Leu
NM_001040167.2:c.562T>C MANE Select	NP_001035257.1:p.Phe188Leu
NM_001040168.2:c.562T>C	NP_001035258.1:p.Phe188Leu
NM_001166355.2:c.349T>C	NP_001159827.1:p.Phe117Leu
NM_002304.3:c.175T>C	NP_002295.1:p.Phe59Leu