Canonical Allele Identifier: CA2656036999

Gene: NF2

Linked Data

• gnomAD v4: 22-29697890-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29697894del , CM000684.2:g.29697894del	GRCh38
NC_000022.10:g.30093883del , CM000684.1:g.30093883del	GRCh37
NC_000022.9:g.28423883del	NCBI36
NG_009057.1:g.99339del , LRG_511:g.99339del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338641.10:c.*3092del MANE Select	ENSP00000344666.5:n.*3092del
ENST00000672896.1:c.*3152del	ENSP00000500117.1:n.*3152del
ENST00000338641.8:c.*3092del	ENSP00000344666.4:n.*3092del
ENST00000361452.8:c.*3152del	ENSP00000354897.4:n.*3152del
ENST00000413209.6:c.*3092del	ENSP00000409921.2:n.*3092del
NM_000268.3:c.*3092del , LRG_511t1:c.*3092del	NP_000259.1:n.*3092del
NM_016418.5:c.*3152del , LRG_511t2:c.*3152del	NP_057502.2:n.*3152del
NM_181828.2:c.*3152del	NP_861966.1:n.*3152del
NM_181829.2:c.*3152del	NP_861967.1:n.*3152del
NM_181830.2:c.*3152del	NP_861968.1:n.*3152del
NM_181832.2:c.*3167del	NP_861970.1:n.*3167del
NM_181833.2:c.*3092del	NP_861971.1:n.*3092del
NR_156186.1:n.5439del
XM_017028810.1:c.*3152del	XP_016884299.1:n.*3152del
NM_000268.4:c.*3092del MANE Select	NP_000259.1:n.*3092del
NM_181828.3:c.*3152del	NP_861966.1:n.*3152del
NM_181829.3:c.*3152del	NP_861967.1:n.*3152del
NM_181830.3:c.*3152del	NP_861968.1:n.*3152del
NM_181832.3:c.*3167del	NP_861970.1:n.*3167del
NR_156186.2:n.5362del
NM_181833.3:c.*3092del	NP_861971.1:n.*3092del