Canonical Allele Identifier: CA411150009

Gene: NF2

Linked Data

• gnomAD v4: 22-29681449-A-C
• MyVariant Identifiers: chr22:g.30077438A>C (hg19) ; chr22:g.29681449A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29681449A>C , CM000684.2:g.29681449A>C	GRCh38
NC_000022.10:g.30077438A>C , CM000684.1:g.30077438A>C	GRCh37
NC_000022.9:g.28407438A>C	NCBI36
NG_009057.1:g.82894A>C , LRG_511:g.82894A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.1450A>C	ENSP00000354529.6:p.Met484Leu
ENST00000673312.2:c.*1079A>C	ENSP00000500186.2:n.*1079A>C
ENST00000338641.10:c.1585A>C MANE Select	ENSP00000344666.5:p.Met529Leu
ENST00000361166.9:c.1003A>C	ENSP00000354529.5:p.Met335Leu
ENST00000672461.1:c.1585A>C	ENSP00000500919.1:p.Met529Leu
ENST00000672805.1:c.*1467A>C	ENSP00000500295.1:n.*1467A>C
ENST00000672896.1:c.1585A>C	ENSP00000500117.1:p.Met529Leu
ENST00000673312.1:c.1604A>C	ENSP00000500186.1:n.1604A>C
ENST00000334961.11:c.1336A>C	ENSP00000335652.7:p.Met446Leu
ENST00000338641.8:c.1585A>C	ENSP00000344666.4:p.Met529Leu
ENST00000353887.8:c.1336A>C	ENSP00000340626.4:p.Met446Leu
ENST00000361166.8:c.1585A>C	ENSP00000354529.4:p.Met529Leu
ENST00000361452.8:c.1462A>C	ENSP00000354897.4:p.Met488Leu
ENST00000361676.8:c.1459A>C	ENSP00000355183.4:p.Met487Leu
ENST00000397789.3:c.1585A>C	ENSP00000380891.3:p.Met529Leu
ENST00000403435.5:c.1498A>C	ENSP00000384029.1:p.Met500Leu
ENST00000403999.7:c.1585A>C	ENSP00000384797.3:p.Met529Leu
ENST00000413209.6:c.448-13303A>C	ENSP00000409921.2:n.448-13303A>C
ENST00000432151.5:c.*93+3126A>C	ENSP00000395885.1:n.*93+3126A>C
NM_000268.3:c.1585A>C , LRG_511t1:c.1585A>C	NP_000259.1:p.Met529Leu
NM_016418.5:c.1585A>C , LRG_511t2:c.1585A>C	NP_057502.2:p.Met529Leu
NM_181825.2:c.1585A>C	NP_861546.1:p.Met529Leu
NM_181828.2:c.1459A>C	NP_861966.1:p.Met487Leu
NM_181829.2:c.1462A>C	NP_861967.1:p.Met488Leu
NM_181830.2:c.1336A>C	NP_861968.1:p.Met446Leu
NM_181831.2:c.1336A>C	NP_861969.1:p.Met446Leu
NM_181832.2:c.1585A>C	NP_861970.1:p.Met529Leu
NM_181833.2:c.448-13303A>C	NP_861971.1:n.448-13303A>C
NR_156186.1:n.2144A>C
XM_017028809.2:c.1471A>C	XP_016884298.1:p.Met491Leu
XM_017028810.1:c.1471A>C	XP_016884299.1:p.Met491Leu
NM_000268.4:c.1585A>C MANE Select	NP_000259.1:p.Met529Leu
NM_181825.3:c.1585A>C	NP_861546.1:p.Met529Leu
NM_181828.3:c.1459A>C	NP_861966.1:p.Met487Leu
NM_181829.3:c.1462A>C	NP_861967.1:p.Met488Leu
NM_181830.3:c.1336A>C	NP_861968.1:p.Met446Leu
NM_181831.3:c.1336A>C	NP_861969.1:p.Met446Leu
NM_181832.3:c.1585A>C	NP_861970.1:p.Met529Leu
NR_156186.2:n.2067A>C
NM_181833.3:c.448-13303A>C	NP_861971.1:n.448-13303A>C