Canonical Allele Identifier: CA2400693238
Gene: NF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29696823_29696840delinsTGTTTTTTTTTTGAGATG , CM000684.2:g.29696823_29696840delinsTGTTTTTTTTTTGAGATG GRCh38
NC_000022.10:g.30092812_30092829delinsTGTTTTTTTTTTGAGATG , CM000684.1:g.30092812_30092829delinsTGTTTTTTTTTTGAGATG GRCh37
NC_000022.9:g.28422812_28422829delinsTGTTTTTTTTTTGAGATG NCBI36
NG_009057.1:g.98268_98285delinsTGTTTTTTTTTTGAGATG , LRG_511:g.98268_98285delinsTGTTTTTTTTTTGAGATG

Transcript Alleles

HGVS Amino-acid change
ENST00000338641.10:c.*2021_*2038delinsTGTTTTTTTTTTGAGATG MANE Select ENSP00000344666.5:n.*2021_*2038delinsTGTT...
ENST00000672461.1:c.*502-438_*502-421delinsTGTTTTTTTTTTGAGATG ENSP00000500919.1:n.*502-438_*502-421deli...
ENST00000672896.1:c.*2081_*2098delinsTGTTTTTTTTTTGAGATG ENSP00000500117.1:n.*2081_*2098delinsTGTT...
ENST00000338641.8:c.*2021_*2038delinsTGTTTTTTTTTTGAGATG ENSP00000344666.4:n.*2021_*2038delinsTGTT...
ENST00000361452.8:c.*2081_*2098delinsTGTTTTTTTTTTGAGATG ENSP00000354897.4:n.*2081_*2098delinsTGTT...
ENST00000413209.6:c.*2021_*2038delinsTGTTTTTTTTTTGAGATG ENSP00000409921.2:n.*2021_*2038delinsTGTT...
NM_000268.3:c.*2021_*2038delinsTGTTTTTTTTTTGAGATG , LRG_511t1:c.*2021_*2038delinsTGTTTTTTTTTTGAGATG NP_000259.1:n.*2021_*2038delinsTGTTTTTTTT...
NM_016418.5:c.*2081_*2098delinsTGTTTTTTTTTTGAGATG , LRG_511t2:c.*2081_*2098delinsTGTTTTTTTTTTGAGATG NP_057502.2:n.*2081_*2098delinsTGTTTTTTTT...
NM_181828.2:c.*2081_*2098delinsTGTTTTTTTTTTGAGATG NP_861966.1:n.*2081_*2098delinsTGTTTTTTTT...
NM_181829.2:c.*2081_*2098delinsTGTTTTTTTTTTGAGATG NP_861967.1:n.*2081_*2098delinsTGTTTTTTTT...
NM_181830.2:c.*2081_*2098delinsTGTTTTTTTTTTGAGATG NP_861968.1:n.*2081_*2098delinsTGTTTTTTTT...
NM_181832.2:c.*2096_*2113delinsTGTTTTTTTTTTGAGATG NP_861970.1:n.*2096_*2113delinsTGTTTTTTTT...
NM_181833.2:c.*2021_*2038delinsTGTTTTTTTTTTGAGATG NP_861971.1:n.*2021_*2038delinsTGTTTTTTTT...
NR_156186.1:n.4368_4385delinsTGTTTTTTTTTTGAGATG
XM_017028810.1:c.*2081_*2098delinsTGTTTTTTTTTTGAGATG XP_016884299.1:n.*2081_*2098delinsTGTTTTT...
NM_000268.4:c.*2021_*2038delinsTGTTTTTTTTTTGAGATG MANE Select NP_000259.1:n.*2021_*2038delinsTGTTTTTTTT...
NM_181828.3:c.*2081_*2098delinsTGTTTTTTTTTTGAGATG NP_861966.1:n.*2081_*2098delinsTGTTTTTTTT...
NM_181829.3:c.*2081_*2098delinsTGTTTTTTTTTTGAGATG NP_861967.1:n.*2081_*2098delinsTGTTTTTTTT...
NM_181830.3:c.*2081_*2098delinsTGTTTTTTTTTTGAGATG NP_861968.1:n.*2081_*2098delinsTGTTTTTTTT...
NM_181832.3:c.*2096_*2113delinsTGTTTTTTTTTTGAGATG NP_861970.1:n.*2096_*2113delinsTGTTTTTTTT...
NR_156186.2:n.4291_4308delinsTGTTTTTTTTTTGAGATG
NM_181833.3:c.*2021_*2038delinsTGTTTTTTTTTTGAGATG NP_861971.1:n.*2021_*2038delinsTGTTTTTTTT...