Canonical Allele Identifier: CA10587372

Gene: NF2

Linked Data

• ClinVar Variation Id: 262992
• ClinVar RCV Id: RCV000249260 ; RCV002392778 ; RCV001469660
• dbSNP Id: rs373442542
• gnomAD v4: 22-29678219-G-A
• COSMIC: COSM3842439 ; COSM3842440
• MyVariant Identifiers: chr22:g.30074208G>A (hg19) ; chr22:g.29678219G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29678219G>A , CM000684.2:g.29678219G>A	GRCh38
NC_000022.10:g.30074208G>A , CM000684.1:g.30074208G>A	GRCh37
NC_000022.9:g.28404208G>A	NCBI36
NG_009057.1:g.79664G>A , LRG_511:g.79664G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.1335G>A	ENSP00000354529.6:p.Pro445=
ENST00000673312.2:c.*964G>A	ENSP00000500186.2:n.*964G>A
ENST00000338641.10:c.1470G>A MANE Select	ENSP00000344666.5:p.Pro490=
ENST00000361166.9:c.888G>A	ENSP00000354529.5:p.Pro296=
ENST00000672461.1:c.1470G>A	ENSP00000500919.1:p.Pro490=
ENST00000672805.1:c.*1352G>A	ENSP00000500295.1:n.*1352G>A
ENST00000672896.1:c.1470G>A	ENSP00000500117.1:p.Pro490=
ENST00000673312.1:c.1489G>A	ENSP00000500186.1:n.1489G>A
ENST00000334961.11:c.1221G>A	ENSP00000335652.7:p.Pro407=
ENST00000338641.8:c.1470G>A	ENSP00000344666.4:p.Pro490=
ENST00000353887.8:c.1221G>A	ENSP00000340626.4:p.Pro407=
ENST00000361166.8:c.1470G>A	ENSP00000354529.4:p.Pro490=
ENST00000361452.8:c.1347G>A	ENSP00000354897.4:p.Pro449=
ENST00000361676.8:c.1344G>A	ENSP00000355183.4:p.Pro448=
ENST00000397789.3:c.1470G>A	ENSP00000380891.3:p.Pro490=
ENST00000403435.5:c.1383G>A	ENSP00000384029.1:p.Pro461=
ENST00000403999.7:c.1470G>A	ENSP00000384797.3:p.Pro490=
ENST00000413209.6:c.448-16533G>A	ENSP00000409921.2:n.448-16533G>A
ENST00000432151.5:c.652G>A	ENSP00000395885.1:p.Val218Ile
NM_000268.3:c.1470G>A , LRG_511t1:c.1470G>A	NP_000259.1:p.Pro490=
NM_016418.5:c.1470G>A , LRG_511t2:c.1470G>A	NP_057502.2:p.Pro490=
NM_181825.2:c.1470G>A	NP_861546.1:p.Pro490=
NM_181828.2:c.1344G>A	NP_861966.1:p.Pro448=
NM_181829.2:c.1347G>A	NP_861967.1:p.Pro449=
NM_181830.2:c.1221G>A	NP_861968.1:p.Pro407=
NM_181831.2:c.1221G>A	NP_861969.1:p.Pro407=
NM_181832.2:c.1470G>A	NP_861970.1:p.Pro490=
NM_181833.2:c.448-16533G>A	NP_861971.1:n.448-16533G>A
NR_156186.1:n.2029G>A
XM_017028809.2:c.1356G>A	XP_016884298.1:p.Pro452=
XM_017028810.1:c.1356G>A	XP_016884299.1:p.Pro452=
NM_000268.4:c.1470G>A MANE Select	NP_000259.1:p.Pro490=
NM_181825.3:c.1470G>A	NP_861546.1:p.Pro490=
NM_181828.3:c.1344G>A	NP_861966.1:p.Pro448=
NM_181829.3:c.1347G>A	NP_861967.1:p.Pro449=
NM_181830.3:c.1221G>A	NP_861968.1:p.Pro407=
NM_181831.3:c.1221G>A	NP_861969.1:p.Pro407=
NM_181832.3:c.1470G>A	NP_861970.1:p.Pro490=
NR_156186.2:n.1952G>A
NM_181833.3:c.448-16533G>A	NP_861971.1:n.448-16533G>A