Canonical Allele Identifier: CA411149678

Gene: NF2

Linked Data

• MyVariant Identifiers: chr22:g.30074251C>G (hg19) ; chr22:g.29678262C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29678262C>G , CM000684.2:g.29678262C>G	GRCh38
NC_000022.10:g.30074251C>G , CM000684.1:g.30074251C>G	GRCh37
NC_000022.9:g.28404251C>G	NCBI36
NG_009057.1:g.79707C>G , LRG_511:g.79707C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.1378C>G	ENSP00000354529.6:p.Leu460Val
ENST00000673312.2:c.*1007C>G	ENSP00000500186.2:n.*1007C>G
ENST00000338641.10:c.1513C>G MANE Select	ENSP00000344666.5:p.Leu505Val
ENST00000361166.9:c.931C>G	ENSP00000354529.5:p.Leu311Val
ENST00000672461.1:c.1513C>G	ENSP00000500919.1:p.Leu505Val
ENST00000672805.1:c.*1395C>G	ENSP00000500295.1:n.*1395C>G
ENST00000672896.1:c.1513C>G	ENSP00000500117.1:p.Leu505Val
ENST00000673312.1:c.1532C>G	ENSP00000500186.1:n.1532C>G
ENST00000334961.11:c.1264C>G	ENSP00000335652.7:p.Leu422Val
ENST00000338641.8:c.1513C>G	ENSP00000344666.4:p.Leu505Val
ENST00000353887.8:c.1264C>G	ENSP00000340626.4:p.Leu422Val
ENST00000361166.8:c.1513C>G	ENSP00000354529.4:p.Leu505Val
ENST00000361452.8:c.1390C>G	ENSP00000354897.4:p.Leu464Val
ENST00000361676.8:c.1387C>G	ENSP00000355183.4:p.Leu463Val
ENST00000397789.3:c.1513C>G	ENSP00000380891.3:p.Leu505Val
ENST00000403435.5:c.1426C>G	ENSP00000384029.1:p.Leu476Val
ENST00000403999.7:c.1513C>G	ENSP00000384797.3:p.Leu505Val
ENST00000413209.6:c.448-16490C>G	ENSP00000409921.2:n.448-16490C>G
ENST00000432151.5:c.*32C>G	ENSP00000395885.1:n.*32C>G
NM_000268.3:c.1513C>G , LRG_511t1:c.1513C>G	NP_000259.1:p.Leu505Val
NM_016418.5:c.1513C>G , LRG_511t2:c.1513C>G	NP_057502.2:p.Leu505Val
NM_181825.2:c.1513C>G	NP_861546.1:p.Leu505Val
NM_181828.2:c.1387C>G	NP_861966.1:p.Leu463Val
NM_181829.2:c.1390C>G	NP_861967.1:p.Leu464Val
NM_181830.2:c.1264C>G	NP_861968.1:p.Leu422Val
NM_181831.2:c.1264C>G	NP_861969.1:p.Leu422Val
NM_181832.2:c.1513C>G	NP_861970.1:p.Leu505Val
NM_181833.2:c.448-16490C>G	NP_861971.1:n.448-16490C>G
NR_156186.1:n.2072C>G
XM_017028809.2:c.1399C>G	XP_016884298.1:p.Leu467Val
XM_017028810.1:c.1399C>G	XP_016884299.1:p.Leu467Val
NM_000268.4:c.1513C>G MANE Select	NP_000259.1:p.Leu505Val
NM_181825.3:c.1513C>G	NP_861546.1:p.Leu505Val
NM_181828.3:c.1387C>G	NP_861966.1:p.Leu463Val
NM_181829.3:c.1390C>G	NP_861967.1:p.Leu464Val
NM_181830.3:c.1264C>G	NP_861968.1:p.Leu422Val
NM_181831.3:c.1264C>G	NP_861969.1:p.Leu422Val
NM_181832.3:c.1513C>G	NP_861970.1:p.Leu505Val
NR_156186.2:n.1995C>G
NM_181833.3:c.448-16490C>G	NP_861971.1:n.448-16490C>G