Canonical Allele Identifier: CA10650991

Gene: NF2

Linked Data

• ClinVar Variation Id: 341091
• ClinVar RCV Id: RCV000266415
• dbSNP Id: rs543669369
• gnomAD v2: 22-30091364-C-T
• gnomAD v3: 22-29695375-C-T
• gnomAD v4: 22-29695375-C-T
• MyVariant Identifiers: chr22:g.30091364C>T (hg19) ; chr22:g.29695375C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29695375C>T , CM000684.2:g.29695375C>T	GRCh38
NC_000022.10:g.30091364C>T , CM000684.1:g.30091364C>T	GRCh37
NC_000022.9:g.28421364C>T	NCBI36
NG_009057.1:g.96820C>T , LRG_511:g.96820C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000338641.10:c.*573C>T MANE Select	ENSP00000344666.5:n.*573C>T
ENST00000672461.1:c.*501+132C>T	ENSP00000500919.1:n.*501+132C>T
ENST00000672896.1:c.*633C>T	ENSP00000500117.1:n.*633C>T
ENST00000338641.8:c.*573C>T	ENSP00000344666.4:n.*573C>T
ENST00000361452.8:c.*633C>T	ENSP00000354897.4:n.*633C>T
ENST00000413209.6:c.*573C>T	ENSP00000409921.2:n.*573C>T
NM_000268.3:c.*573C>T , LRG_511t1:c.*573C>T	NP_000259.1:n.*573C>T
NM_016418.5:c.*633C>T , LRG_511t2:c.*633C>T	NP_057502.2:n.*633C>T
NM_181828.2:c.*633C>T	NP_861966.1:n.*633C>T
NM_181829.2:c.*633C>T	NP_861967.1:n.*633C>T
NM_181830.2:c.*633C>T	NP_861968.1:n.*633C>T
NM_181832.2:c.*648C>T	NP_861970.1:n.*648C>T
NM_181833.2:c.*573C>T	NP_861971.1:n.*573C>T
NR_156186.1:n.2920C>T
XM_017028810.1:c.*633C>T	XP_016884299.1:n.*633C>T
NM_000268.4:c.*573C>T MANE Select	NP_000259.1:n.*573C>T
NM_181828.3:c.*633C>T	NP_861966.1:n.*633C>T
NM_181829.3:c.*633C>T	NP_861967.1:n.*633C>T
NM_181830.3:c.*633C>T	NP_861968.1:n.*633C>T
NM_181832.3:c.*648C>T	NP_861970.1:n.*648C>T
NR_156186.2:n.2843C>T
NM_181833.3:c.*573C>T	NP_861971.1:n.*573C>T