Canonical Allele Identifier: CA514185980

Gene: NF2

Linked Data

• gnomAD v4: 22-29673319-C-A
• MyVariant Identifiers: chr22:g.30069308C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29673319C>A , CM000684.2:g.29673319C>A	GRCh38
NC_000022.10:g.30069308C>A , CM000684.1:g.30069308C>A	GRCh37
NC_000022.9:g.28399308C>A	NCBI36
NG_009057.1:g.74764C>A , LRG_511:g.74764C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000361166.10:c.1038C>A	ENSP00000354529.6:p.Thr346=
ENST00000673312.2:c.*667C>A	ENSP00000500186.2:n.*667C>A
ENST00000338641.10:c.1173C>A MANE Select	ENSP00000344666.5:p.Thr391=
ENST00000361166.9:c.591C>A	ENSP00000354529.5:p.Thr197=
ENST00000672461.1:c.1173C>A	ENSP00000500919.1:p.Thr391=
ENST00000672805.1:c.*1055C>A	ENSP00000500295.1:n.*1055C>A
ENST00000672896.1:c.1173C>A	ENSP00000500117.1:p.Thr391=
ENST00000673312.1:c.1192C>A	ENSP00000500186.1:n.1192C>A
ENST00000334961.11:c.924C>A	ENSP00000335652.7:p.Thr308=
ENST00000338641.8:c.1173C>A	ENSP00000344666.4:p.Thr391=
ENST00000353887.8:c.924C>A	ENSP00000340626.4:p.Thr308=
ENST00000361166.8:c.1173C>A	ENSP00000354529.4:p.Thr391=
ENST00000361452.8:c.1050C>A	ENSP00000354897.4:p.Thr350=
ENST00000361676.8:c.1047C>A	ENSP00000355183.4:p.Thr349=
ENST00000397789.3:c.1173C>A	ENSP00000380891.3:p.Thr391=
ENST00000403435.5:c.1086C>A	ENSP00000384029.1:p.Thr362=
ENST00000403999.7:c.1173C>A	ENSP00000384797.3:p.Thr391=
ENST00000413209.6:c.448-21433C>A	ENSP00000409921.2:n.448-21433C>A
ENST00000432151.5:c.523-1517C>A	ENSP00000395885.1:n.523-1517C>A
NM_000268.3:c.1173C>A , LRG_511t1:c.1173C>A	NP_000259.1:p.Thr391=
NM_016418.5:c.1173C>A , LRG_511t2:c.1173C>A	NP_057502.2:p.Thr391=
NM_181825.2:c.1173C>A	NP_861546.1:p.Thr391=
NM_181828.2:c.1047C>A	NP_861966.1:p.Thr349=
NM_181829.2:c.1050C>A	NP_861967.1:p.Thr350=
NM_181830.2:c.924C>A	NP_861968.1:p.Thr308=
NM_181831.2:c.924C>A	NP_861969.1:p.Thr308=
NM_181832.2:c.1173C>A	NP_861970.1:p.Thr391=
NM_181833.2:c.448-21433C>A	NP_861971.1:n.448-21433C>A
NR_156186.1:n.1732C>A
XM_017028809.2:c.1059C>A	XP_016884298.1:p.Thr353=
XM_017028810.1:c.1059C>A	XP_016884299.1:p.Thr353=
NM_000268.4:c.1173C>A MANE Select	NP_000259.1:p.Thr391=
NM_181825.3:c.1173C>A	NP_861546.1:p.Thr391=
NM_181828.3:c.1047C>A	NP_861966.1:p.Thr349=
NM_181829.3:c.1050C>A	NP_861967.1:p.Thr350=
NM_181830.3:c.924C>A	NP_861968.1:p.Thr308=
NM_181831.3:c.924C>A	NP_861969.1:p.Thr308=
NM_181832.3:c.1173C>A	NP_861970.1:p.Thr391=
NR_156186.2:n.1655C>A
NM_181833.3:c.448-21433C>A	NP_861971.1:n.448-21433C>A