Canonical Allele Identifier: CA411148240

Gene: NF2

Linked Data

• MyVariant Identifiers: chr22:g.30069362G>T (hg19) ; chr22:g.29673373G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29673373G>T , CM000684.2:g.29673373G>T	GRCh38
NC_000022.10:g.30069362G>T , CM000684.1:g.30069362G>T	GRCh37
NC_000022.9:g.28399362G>T	NCBI36
NG_009057.1:g.74818G>T , LRG_511:g.74818G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.1092G>T	ENSP00000354529.6:p.Met364Ile
ENST00000673312.2:c.*721G>T	ENSP00000500186.2:n.*721G>T
ENST00000338641.10:c.1227G>T MANE Select	ENSP00000344666.5:p.Met409Ile
ENST00000361166.9:c.645G>T	ENSP00000354529.5:p.Met215Ile
ENST00000672461.1:c.1227G>T	ENSP00000500919.1:p.Met409Ile
ENST00000672805.1:c.*1109G>T	ENSP00000500295.1:n.*1109G>T
ENST00000672896.1:c.1227G>T	ENSP00000500117.1:p.Met409Ile
ENST00000673312.1:c.1246G>T	ENSP00000500186.1:n.1246G>T
ENST00000334961.11:c.978G>T	ENSP00000335652.7:p.Met326Ile
ENST00000338641.8:c.1227G>T	ENSP00000344666.4:p.Met409Ile
ENST00000353887.8:c.978G>T	ENSP00000340626.4:p.Met326Ile
ENST00000361166.8:c.1227G>T	ENSP00000354529.4:p.Met409Ile
ENST00000361452.8:c.1104G>T	ENSP00000354897.4:p.Met368Ile
ENST00000361676.8:c.1101G>T	ENSP00000355183.4:p.Met367Ile
ENST00000397789.3:c.1227G>T	ENSP00000380891.3:p.Met409Ile
ENST00000403435.5:c.1140G>T	ENSP00000384029.1:p.Met380Ile
ENST00000403999.7:c.1227G>T	ENSP00000384797.3:p.Met409Ile
ENST00000413209.6:c.448-21379G>T	ENSP00000409921.2:n.448-21379G>T
ENST00000432151.5:c.523-1463G>T	ENSP00000395885.1:n.523-1463G>T
NM_000268.3:c.1227G>T , LRG_511t1:c.1227G>T	NP_000259.1:p.Met409Ile
NM_016418.5:c.1227G>T , LRG_511t2:c.1227G>T	NP_057502.2:p.Met409Ile
NM_181825.2:c.1227G>T	NP_861546.1:p.Met409Ile
NM_181828.2:c.1101G>T	NP_861966.1:p.Met367Ile
NM_181829.2:c.1104G>T	NP_861967.1:p.Met368Ile
NM_181830.2:c.978G>T	NP_861968.1:p.Met326Ile
NM_181831.2:c.978G>T	NP_861969.1:p.Met326Ile
NM_181832.2:c.1227G>T	NP_861970.1:p.Met409Ile
NM_181833.2:c.448-21379G>T	NP_861971.1:n.448-21379G>T
NR_156186.1:n.1786G>T
XM_017028809.2:c.1113G>T	XP_016884298.1:p.Met371Ile
XM_017028810.1:c.1113G>T	XP_016884299.1:p.Met371Ile
NM_000268.4:c.1227G>T MANE Select	NP_000259.1:p.Met409Ile
NM_181825.3:c.1227G>T	NP_861546.1:p.Met409Ile
NM_181828.3:c.1101G>T	NP_861966.1:p.Met367Ile
NM_181829.3:c.1104G>T	NP_861967.1:p.Met368Ile
NM_181830.3:c.978G>T	NP_861968.1:p.Met326Ile
NM_181831.3:c.978G>T	NP_861969.1:p.Met326Ile
NM_181832.3:c.1227G>T	NP_861970.1:p.Met409Ile
NR_156186.2:n.1709G>T
NM_181833.3:c.448-21379G>T	NP_861971.1:n.448-21379G>T