Canonical Allele Identifier: CA2656037039

Gene: NF2

Linked Data

• gnomAD v4: 22-29697940-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29697941dup , CM000684.2:g.29697941dup	GRCh38
NC_000022.10:g.30093930dup , CM000684.1:g.30093930dup	GRCh37
NC_000022.9:g.28423930dup	NCBI36
NG_009057.1:g.99386dup , LRG_511:g.99386dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338641.10:c.*3139dup MANE Select	ENSP00000344666.5:n.*3139dup
ENST00000672896.1:c.*3199dup	ENSP00000500117.1:n.*3199dup
ENST00000338641.8:c.*3139dup	ENSP00000344666.4:n.*3139dup
ENST00000361452.8:c.*3199dup	ENSP00000354897.4:n.*3199dup
ENST00000413209.6:c.*3139dup	ENSP00000409921.2:n.*3139dup
NM_000268.3:c.*3139dup , LRG_511t1:c.*3139dup	NP_000259.1:n.*3139dup
NM_016418.5:c.*3199dup , LRG_511t2:c.*3199dup	NP_057502.2:n.*3199dup
NM_181828.2:c.*3199dup	NP_861966.1:n.*3199dup
NM_181829.2:c.*3199dup	NP_861967.1:n.*3199dup
NM_181830.2:c.*3199dup	NP_861968.1:n.*3199dup
NM_181832.2:c.*3214dup	NP_861970.1:n.*3214dup
NM_181833.2:c.*3139dup	NP_861971.1:n.*3139dup
NR_156186.1:n.5486dup
XM_017028810.1:c.*3199dup	XP_016884299.1:n.*3199dup
NM_000268.4:c.*3139dup MANE Select	NP_000259.1:n.*3139dup
NM_181828.3:c.*3199dup	NP_861966.1:n.*3199dup
NM_181829.3:c.*3199dup	NP_861967.1:n.*3199dup
NM_181830.3:c.*3199dup	NP_861968.1:n.*3199dup
NM_181832.3:c.*3214dup	NP_861970.1:n.*3214dup
NR_156186.2:n.5409dup
NM_181833.3:c.*3139dup	NP_861971.1:n.*3139dup