Canonical Allele Identifier: CA2656036099

Gene: NF2

Linked Data

• gnomAD v4: 22-29696904-C-CAG

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29696904_29696905insAG , CM000684.2:g.29696904_29696905insAG	GRCh38
NC_000022.10:g.30092893_30092894insAG , CM000684.1:g.30092893_30092894insAG	GRCh37
NC_000022.9:g.28422893_28422894insAG	NCBI36
NG_009057.1:g.98349_98350insAG , LRG_511:g.98349_98350insAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000338641.10:c.*2102_*2103insAG MANE Select	ENSP00000344666.5:n.*2102_*2103insAG
ENST00000672461.1:c.*502-357_*502-356insAG	ENSP00000500919.1:n.*502-357_*502-356insAG
ENST00000672896.1:c.*2162_*2163insAG	ENSP00000500117.1:n.*2162_*2163insAG
ENST00000338641.8:c.*2102_*2103insAG	ENSP00000344666.4:n.*2102_*2103insAG
ENST00000361452.8:c.*2162_*2163insAG	ENSP00000354897.4:n.*2162_*2163insAG
ENST00000413209.6:c.*2102_*2103insAG	ENSP00000409921.2:n.*2102_*2103insAG
NM_000268.3:c.*2102_*2103insAG , LRG_511t1:c.*2102_*2103insAG	NP_000259.1:n.*2102_*2103insAG
NM_016418.5:c.*2162_*2163insAG , LRG_511t2:c.*2162_*2163insAG	NP_057502.2:n.*2162_*2163insAG
NM_181828.2:c.*2162_*2163insAG	NP_861966.1:n.*2162_*2163insAG
NM_181829.2:c.*2162_*2163insAG	NP_861967.1:n.*2162_*2163insAG
NM_181830.2:c.*2162_*2163insAG	NP_861968.1:n.*2162_*2163insAG
NM_181832.2:c.*2177_*2178insAG	NP_861970.1:n.*2177_*2178insAG
NM_181833.2:c.*2102_*2103insAG	NP_861971.1:n.*2102_*2103insAG
NR_156186.1:n.4449_4450insAG
XM_017028810.1:c.*2162_*2163insAG	XP_016884299.1:n.*2162_*2163insAG
NM_000268.4:c.*2102_*2103insAG MANE Select	NP_000259.1:n.*2102_*2103insAG
NM_181828.3:c.*2162_*2163insAG	NP_861966.1:n.*2162_*2163insAG
NM_181829.3:c.*2162_*2163insAG	NP_861967.1:n.*2162_*2163insAG
NM_181830.3:c.*2162_*2163insAG	NP_861968.1:n.*2162_*2163insAG
NM_181832.3:c.*2177_*2178insAG	NP_861970.1:n.*2177_*2178insAG
NR_156186.2:n.4372_4373insAG
NM_181833.3:c.*2102_*2103insAG	NP_861971.1:n.*2102_*2103insAG