Canonical Allele Identifier: CA2400653192
Gene: NF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29603586C= , CM000684.2:g.29603586C= GRCh38
NC_000022.10:g.29999575C= , CM000684.1:g.29999575C= GRCh37
NC_000022.9:g.28329575C= NCBI36
NG_009057.1:g.5031C= , LRG_511:g.5031C=

Transcript Alleles

HGVS Amino-acid change
ENST00000672805.1:c.-413C= ENSP00000500295.1:n.-413C=
ENST00000338641.8:c.-413C= ENSP00000344666.4:n.-413C=
ENST00000413209.6:c.-413C= ENSP00000409921.2:n.-413C=
NM_000268.3:c.-413C= , LRG_511t1:c.-413C= NP_000259.1:n.-413C=
NM_016418.5:c.-413C= , LRG_511t2:c.-413C= NP_057502.2:n.-413C=
NM_181825.2:c.-413C= NP_861546.1:n.-413C=
NM_181828.2:c.-413C= NP_861966.1:n.-413C=
NM_181829.2:c.-413C= NP_861967.1:n.-413C=
NM_181830.2:c.-413C= NP_861968.1:n.-413C=
NM_181831.2:c.-413C= NP_861969.1:n.-413C=
NM_181832.2:c.-413C= NP_861970.1:n.-413C=
NM_181833.2:c.-413C= NP_861971.1:n.-413C=
NR_156186.1:n.31C=