Canonical Allele Identifier: CA2637074938

Gene: NF1

Linked Data

• gnomAD v4: 17-31214515-CAAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31214519_31214521del , CM000679.2:g.31214519_31214521del	GRCh38
NC_000017.10:g.29541537_29541539del , CM000679.1:g.29541537_29541539del	GRCh37
NC_000017.9:g.26565663_26565665del	NCBI36
NG_009018.1:g.124543_124545del , LRG_214:g.124543_124545del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.1506_1508del	ENSP00000512431.1:p.Arg502del
ENST00000686189.1:c.906_908del	ENSP00000509682.1:p.Arg302del
ENST00000691014.1:c.1491_1493del	ENSP00000510595.1:p.Arg497del
ENST00000358273.9:c.1461_1463del MANE Select	ENSP00000351015.4:p.Arg487del
ENST00000356175.7:c.1461_1463del	ENSP00000348498.3:p.Arg487del
ENST00000358273.8:c.1461_1463del	ENSP00000351015.4:p.Arg487del
ENST00000431387.8:c.1461_1463del	ENSP00000412921.4:p.Arg487del
ENST00000456735.6:c.459_461del	ENSP00000389907.2:p.Arg153del
ENST00000487476.5:n.1844_1846del
ENST00000495910.6:c.1236_1238del
ENST00000579081.5:c.1563_1565del	ENSP00000462408.1:p.Arg521del
NM_000267.3:c.1461_1463del , LRG_214t1:c.1461_1463del	NP_000258.1:p.Arg487del
NM_001042492.2:c.1461_1463del , LRG_214t2:c.1461_1463del	NP_001035957.1:p.Arg487del
NM_001128147.2:c.1461_1463del	NP_001121619.1:p.Arg487del
XM_005257983.1:c.1461_1463del	XP_005258040.1:p.Arg487del
XM_005257984.1:c.1461_1463del	XP_005258041.1:p.Arg487del
XM_006721922.1:c.1491_1493del	XP_006721985.1:p.Arg497del
XM_006721923.2:c.1452_1454del	XP_006721986.1:p.Arg484del
XM_006721924.1:c.1491_1493del	XP_006721987.1:p.Arg497del
XM_006721925.1:c.1491_1493del	XP_006721988.1:p.Arg497del
XM_006721926.2:c.1491_1493del	XP_006721989.1:p.Arg497del
XM_006721927.1:c.1491_1493del	XP_006721990.1:p.Arg497del
XM_006721928.2:c.1491_1493del	XP_006721991.1:p.Arg497del
XM_011524852.1:c.1491_1493del	XP_011523154.1:p.Arg497del
XM_011524853.1:c.1452_1454del	XP_011523155.1:p.Arg484del
XM_011524854.1:c.1452_1454del	XP_011523156.1:p.Arg484del
XM_011524855.1:c.1452_1454del	XP_011523157.1:p.Arg484del
XM_011524856.1:c.1452_1454del	XP_011523158.1:p.Arg484del
XM_011524857.1:c.1491_1493del	XP_011523159.1:p.Arg497del
NM_001042492.3:c.1461_1463del MANE Select	NP_001035957.1:p.Arg487del
NM_001128147.3:c.1461_1463del	NP_001121619.1:p.Arg487del