Canonical Allele Identifier: CA1024929309

Gene: NF2

Linked Data

• dbSNP Id: rs142797364
• gnomAD v3: 22-29697643-C-A
• gnomAD v4: 22-29697643-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29697643C>A , CM000684.2:g.29697643C>A	GRCh38
NC_000022.10:g.30093632C>A , CM000684.1:g.30093632C>A	GRCh37
NC_000022.9:g.28423632C>A	NCBI36
NG_009057.1:g.99088C>A , LRG_511:g.99088C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000338641.10:c.*2841C>A MANE Select	ENSP00000344666.5:n.*2841C>A
ENST00000672896.1:c.*2901C>A	ENSP00000500117.1:n.*2901C>A
ENST00000338641.8:c.*2841C>A	ENSP00000344666.4:n.*2841C>A
ENST00000361452.8:c.*2901C>A	ENSP00000354897.4:n.*2901C>A
ENST00000413209.6:c.*2841C>A	ENSP00000409921.2:n.*2841C>A
NM_000268.3:c.*2841C>A , LRG_511t1:c.*2841C>A	NP_000259.1:n.*2841C>A
NM_016418.5:c.*2901C>A , LRG_511t2:c.*2901C>A	NP_057502.2:n.*2901C>A
NM_181828.2:c.*2901C>A	NP_861966.1:n.*2901C>A
NM_181829.2:c.*2901C>A	NP_861967.1:n.*2901C>A
NM_181830.2:c.*2901C>A	NP_861968.1:n.*2901C>A
NM_181832.2:c.*2916C>A	NP_861970.1:n.*2916C>A
NM_181833.2:c.*2841C>A	NP_861971.1:n.*2841C>A
NR_156186.1:n.5188C>A
XM_017028810.1:c.*2901C>A	XP_016884299.1:n.*2901C>A
NM_000268.4:c.*2841C>A MANE Select	NP_000259.1:n.*2841C>A
NM_181828.3:c.*2901C>A	NP_861966.1:n.*2901C>A
NM_181829.3:c.*2901C>A	NP_861967.1:n.*2901C>A
NM_181830.3:c.*2901C>A	NP_861968.1:n.*2901C>A
NM_181832.3:c.*2916C>A	NP_861970.1:n.*2916C>A
NR_156186.2:n.5111C>A
NM_181833.3:c.*2841C>A	NP_861971.1:n.*2841C>A