Canonical Allele Identifier: CA2400692506
Gene: NF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29695234T= , CM000684.2:g.29695234T= GRCh38
NC_000022.10:g.30091223T= , CM000684.1:g.30091223T= GRCh37
NC_000022.9:g.28421223T= NCBI36
NG_009057.1:g.96679T= , LRG_511:g.96679T=

Transcript Alleles

HGVS Amino-acid change
ENST00000338641.10:c.*432T= MANE Select ENSP00000344666.5:n.*432T=
ENST00000672461.1:c.*492T= ENSP00000500919.1:n.*492T=
ENST00000672896.1:c.*492T= ENSP00000500117.1:n.*492T=
ENST00000338641.8:c.*432T= ENSP00000344666.4:n.*432T=
ENST00000361452.8:c.*492T= ENSP00000354897.4:n.*492T=
ENST00000413209.6:c.*432T= ENSP00000409921.2:n.*432T=
NM_000268.3:c.*432T= , LRG_511t1:c.*432T= NP_000259.1:n.*432T=
NM_016418.5:c.*492T= , LRG_511t2:c.*492T= NP_057502.2:n.*492T=
NM_181828.2:c.*492T= NP_861966.1:n.*492T=
NM_181829.2:c.*492T= NP_861967.1:n.*492T=
NM_181830.2:c.*492T= NP_861968.1:n.*492T=
NM_181832.2:c.*507T= NP_861970.1:n.*507T=
NM_181833.2:c.*432T= NP_861971.1:n.*432T=
NR_156186.1:n.2779T=
XM_017028810.1:c.*492T= XP_016884299.1:n.*492T=
NM_000268.4:c.*432T= MANE Select NP_000259.1:n.*432T=
NM_181828.3:c.*492T= NP_861966.1:n.*492T=
NM_181829.3:c.*492T= NP_861967.1:n.*492T=
NM_181830.3:c.*492T= NP_861968.1:n.*492T=
NM_181832.3:c.*507T= NP_861970.1:n.*507T=
NR_156186.2:n.2702T=
NM_181833.3:c.*432T= NP_861971.1:n.*432T=