Canonical Allele Identifier: CA411149718

Gene: NF2

Linked Data

• gnomAD v4: 22-29678280-G-T
• MyVariant Identifiers: chr22:g.30074269G>T (hg19) ; chr22:g.29678280G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29678280G>T , CM000684.2:g.29678280G>T	GRCh38
NC_000022.10:g.30074269G>T , CM000684.1:g.30074269G>T	GRCh37
NC_000022.9:g.28404269G>T	NCBI36
NG_009057.1:g.79725G>T , LRG_511:g.79725G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000361166.10:c.1396G>T	ENSP00000354529.6:p.Asp466Tyr
ENST00000673312.2:c.*1025G>T	ENSP00000500186.2:n.*1025G>T
ENST00000338641.10:c.1531G>T MANE Select	ENSP00000344666.5:p.Asp511Tyr
ENST00000361166.9:c.949G>T	ENSP00000354529.5:p.Asp317Tyr
ENST00000672461.1:c.1531G>T	ENSP00000500919.1:p.Asp511Tyr
ENST00000672805.1:c.*1413G>T	ENSP00000500295.1:n.*1413G>T
ENST00000672896.1:c.1531G>T	ENSP00000500117.1:p.Asp511Tyr
ENST00000673312.1:c.1550G>T	ENSP00000500186.1:n.1550G>T
ENST00000334961.11:c.1282G>T	ENSP00000335652.7:p.Asp428Tyr
ENST00000338641.8:c.1531G>T	ENSP00000344666.4:p.Asp511Tyr
ENST00000353887.8:c.1282G>T	ENSP00000340626.4:p.Asp428Tyr
ENST00000361166.8:c.1531G>T	ENSP00000354529.4:p.Asp511Tyr
ENST00000361452.8:c.1408G>T	ENSP00000354897.4:p.Asp470Tyr
ENST00000361676.8:c.1405G>T	ENSP00000355183.4:p.Asp469Tyr
ENST00000397789.3:c.1531G>T	ENSP00000380891.3:p.Asp511Tyr
ENST00000403435.5:c.1444G>T	ENSP00000384029.1:p.Asp482Tyr
ENST00000403999.7:c.1531G>T	ENSP00000384797.3:p.Asp511Tyr
ENST00000413209.6:c.448-16472G>T	ENSP00000409921.2:n.448-16472G>T
ENST00000432151.5:c.*50G>T	ENSP00000395885.1:n.*50G>T
NM_000268.3:c.1531G>T , LRG_511t1:c.1531G>T	NP_000259.1:p.Asp511Tyr
NM_016418.5:c.1531G>T , LRG_511t2:c.1531G>T	NP_057502.2:p.Asp511Tyr
NM_181825.2:c.1531G>T	NP_861546.1:p.Asp511Tyr
NM_181828.2:c.1405G>T	NP_861966.1:p.Asp469Tyr
NM_181829.2:c.1408G>T	NP_861967.1:p.Asp470Tyr
NM_181830.2:c.1282G>T	NP_861968.1:p.Asp428Tyr
NM_181831.2:c.1282G>T	NP_861969.1:p.Asp428Tyr
NM_181832.2:c.1531G>T	NP_861970.1:p.Asp511Tyr
NM_181833.2:c.448-16472G>T	NP_861971.1:n.448-16472G>T
NR_156186.1:n.2090G>T
XM_017028809.2:c.1417G>T	XP_016884298.1:p.Asp473Tyr
XM_017028810.1:c.1417G>T	XP_016884299.1:p.Asp473Tyr
NM_000268.4:c.1531G>T MANE Select	NP_000259.1:p.Asp511Tyr
NM_181825.3:c.1531G>T	NP_861546.1:p.Asp511Tyr
NM_181828.3:c.1405G>T	NP_861966.1:p.Asp469Tyr
NM_181829.3:c.1408G>T	NP_861967.1:p.Asp470Tyr
NM_181830.3:c.1282G>T	NP_861968.1:p.Asp428Tyr
NM_181831.3:c.1282G>T	NP_861969.1:p.Asp428Tyr
NM_181832.3:c.1531G>T	NP_861970.1:p.Asp511Tyr
NR_156186.2:n.2013G>T
NM_181833.3:c.448-16472G>T	NP_861971.1:n.448-16472G>T