Canonical Allele Identifier: CA11659069

Gene: FGF2 NUDT6

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122895552T>G , CM000666.2:g.122895552T>G	GRCh38
NC_000004.11:g.123816707T>G , CM000666.1:g.123816707T>G	GRCh37
NC_000004.10:g.124036157T>G	NCBI36
NG_029067.1:g.73845T>G
NG_030404.1:g.32453A>C
NG_029067.2:g.73845T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264498.9:c.*3156T>G (FGF2)	ENSP00000264498.4:n.*3156T>G
ENST00000264498.8:c.*3156T>G (FGF2)	ENSP00000264498.4:n.*3156T>G
ENST00000304430.10:c.553+2072A>C (NUDT6) MANE Select	ENSP00000306070.5:n.553+2072A>C
ENST00000644866.2:c.*3156T>G (FGF2) MANE Select	ENSP00000494222.1:n.*3156T>G
ENST00000264498.7:c.*3156T>G (FGF2)	ENSP00000264498.3:n.*3156T>G
ENST00000304430.9:c.553+2072A>C (NUDT6)	ENSP00000306070.5:n.553+2072A>C
ENST00000339154.6:c.46+2072A>C (NUDT6)	ENSP00000344011.2:n.46+2072A>C
ENST00000502270.5:c.46+2072A>C (NUDT6)	ENSP00000424117.1:n.46+2072A>C
ENST00000503370.5:c.*495-2327A>C (NUDT6)	ENSP00000422698.1:n.*495-2327A>C
ENST00000510735.1:c.163+2072A>C (NUDT6)
ENST00000512116.5:c.*644+2072A>C (NUDT6)	ENSP00000420843.1:n.*644+2072A>C
ENST00000614010.4:c.*3156T>G (FGF2)	ENSP00000478620.1:n.*3156T>G
NM_002006.4:c.*3156T>G (FGF2)	NP_001997.5:n.*3156T>G
NM_007083.4:c.553+2072A>C (NUDT6)	NP_009014.2:n.553+2072A>C
NM_198041.2:c.46+2072A>C (NUDT6)	NP_932158.1:n.46+2072A>C
NM_001361665.1:c.*3156T>G (FGF2)	NP_001348594.1:n.*3156T>G
NM_002006.5:c.*3156T>G (FGF2)	NP_001997.5:n.*3156T>G
NM_001361665.2:c.*3156T>G (FGF2) MANE Select	NP_001348594.1:n.*3156T>G
NM_007083.5:c.553+2072A>C (NUDT6) MANE Select	NP_009014.2:n.553+2072A>C
NM_198041.3:c.46+2072A>C (NUDT6)	NP_932158.1:n.46+2072A>C
NM_002006.6:c.*3156T>G (FGF2)	NP_001997.5:n.*3156T>G