Canonical Allele Identifier: CA2400692354
Gene: NF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29694911G= , CM000684.2:g.29694911G= GRCh38
NC_000022.10:g.30090900G= , CM000684.1:g.30090900G= GRCh37
NC_000022.9:g.28420900G= NCBI36
NG_009057.1:g.96356G= , LRG_511:g.96356G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361166.10:c.*109G= ENSP00000354529.6:n.*109G=
ENST00000673312.2:c.*1391G= ENSP00000500186.2:n.*1391G=
ENST00000338641.10:c.*109G= MANE Select ENSP00000344666.5:n.*109G=
ENST00000361166.9:c.1315G= ENSP00000354529.5:n.1315G=
ENST00000672461.1:c.*169G= ENSP00000500919.1:n.*169G=
ENST00000672805.1:c.*1779G= ENSP00000500295.1:n.*1779G=
ENST00000672896.1:c.*169G= ENSP00000500117.1:n.*169G=
ENST00000673312.1:c.1916G= ENSP00000500186.1:n.1916G=
ENST00000338641.8:c.*109G= ENSP00000344666.4:n.*109G=
ENST00000361452.8:c.*169G= ENSP00000354897.4:n.*169G=
ENST00000413209.6:c.*109G= ENSP00000409921.2:n.*109G=
ENST00000432151.5:c.*253G= ENSP00000395885.1:n.*253G=
NM_000268.3:c.*109G= , LRG_511t1:c.*109G= NP_000259.1:n.*109G=
NM_016418.5:c.*169G= , LRG_511t2:c.*169G= NP_057502.2:n.*169G=
NM_181828.2:c.*169G= NP_861966.1:n.*169G=
NM_181829.2:c.*169G= NP_861967.1:n.*169G=
NM_181830.2:c.*169G= NP_861968.1:n.*169G=
NM_181832.2:c.*184G= NP_861970.1:n.*184G=
NM_181833.2:c.*109G= NP_861971.1:n.*109G=
NR_156186.1:n.2456G=
XM_017028809.2:c.*109G= XP_016884298.1:n.*109G=
XM_017028810.1:c.*169G= XP_016884299.1:n.*169G=
NM_000268.4:c.*109G= MANE Select NP_000259.1:n.*109G=
NM_181828.3:c.*169G= NP_861966.1:n.*169G=
NM_181829.3:c.*169G= NP_861967.1:n.*169G=
NM_181830.3:c.*169G= NP_861968.1:n.*169G=
NM_181832.3:c.*184G= NP_861970.1:n.*184G=
NR_156186.2:n.2379G=
NM_181833.3:c.*109G= NP_861971.1:n.*109G=