Canonical Allele Identifier: CA411146921

Gene: NF2

Linked Data

• dbSNP Id: rs2147072551
• gnomAD v4: 22-29671880-A-G
• MyVariant Identifiers: chr22:g.30067869A>G (hg19) ; chr22:g.29671880A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29671880A>G , CM000684.2:g.29671880A>G	GRCh38
NC_000022.10:g.30067869A>G , CM000684.1:g.30067869A>G	GRCh37
NC_000022.9:g.28397869A>G	NCBI36
NG_009057.1:g.73325A>G , LRG_511:g.73325A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.919A>G	ENSP00000354529.6:p.Thr307Ala
ENST00000673312.2:c.*548A>G	ENSP00000500186.2:n.*548A>G
ENST00000338641.10:c.1054A>G MANE Select	ENSP00000344666.5:p.Thr352Ala
ENST00000361166.9:c.472A>G	ENSP00000354529.5:p.Thr158Ala
ENST00000672461.1:c.1054A>G	ENSP00000500919.1:p.Thr352Ala
ENST00000672805.1:c.*936A>G	ENSP00000500295.1:n.*936A>G
ENST00000672896.1:c.1054A>G	ENSP00000500117.1:p.Thr352Ala
ENST00000673312.1:c.1073A>G	ENSP00000500186.1:n.1073A>G
ENST00000334961.11:c.805A>G	ENSP00000335652.7:p.Thr269Ala
ENST00000338641.8:c.1054A>G	ENSP00000344666.4:p.Thr352Ala
ENST00000353887.8:c.805A>G	ENSP00000340626.4:p.Thr269Ala
ENST00000361166.8:c.1054A>G	ENSP00000354529.4:p.Thr352Ala
ENST00000361452.8:c.931A>G	ENSP00000354897.4:p.Thr311Ala
ENST00000361676.8:c.928A>G	ENSP00000355183.4:p.Thr310Ala
ENST00000397789.3:c.1054A>G	ENSP00000380891.3:p.Thr352Ala
ENST00000403435.5:c.1000-33A>G	ENSP00000384029.1:n.1000-33A>G
ENST00000403999.7:c.1054A>G	ENSP00000384797.3:p.Thr352Ala
ENST00000413209.6:c.448-22872A>G	ENSP00000409921.2:n.448-22872A>G
ENST00000432151.5:c.523-2956A>G	ENSP00000395885.1:n.523-2956A>G
NM_000268.3:c.1054A>G , LRG_511t1:c.1054A>G	NP_000259.1:p.Thr352Ala
NM_016418.5:c.1054A>G , LRG_511t2:c.1054A>G	NP_057502.2:p.Thr352Ala
NM_181825.2:c.1054A>G	NP_861546.1:p.Thr352Ala
NM_181828.2:c.928A>G	NP_861966.1:p.Thr310Ala
NM_181829.2:c.931A>G	NP_861967.1:p.Thr311Ala
NM_181830.2:c.805A>G	NP_861968.1:p.Thr269Ala
NM_181831.2:c.805A>G	NP_861969.1:p.Thr269Ala
NM_181832.2:c.1054A>G	NP_861970.1:p.Thr352Ala
NM_181833.2:c.448-22872A>G	NP_861971.1:n.448-22872A>G
NR_156186.1:n.1613A>G
XM_017028809.2:c.940A>G	XP_016884298.1:p.Thr314Ala
XM_017028810.1:c.940A>G	XP_016884299.1:p.Thr314Ala
NM_000268.4:c.1054A>G MANE Select	NP_000259.1:p.Thr352Ala
NM_181825.3:c.1054A>G	NP_861546.1:p.Thr352Ala
NM_181828.3:c.928A>G	NP_861966.1:p.Thr310Ala
NM_181829.3:c.931A>G	NP_861967.1:p.Thr311Ala
NM_181830.3:c.805A>G	NP_861968.1:p.Thr269Ala
NM_181831.3:c.805A>G	NP_861969.1:p.Thr269Ala
NM_181832.3:c.1054A>G	NP_861970.1:p.Thr352Ala
NR_156186.2:n.1536A>G
NM_181833.3:c.448-22872A>G	NP_861971.1:n.448-22872A>G