Canonical Allele Identifier: CA658656610

Gene: NF1

Linked Data

• ClinVar Variation Id: 457578
• ClinVar RCV Id: RCV000535397 ; RCV002316496 ; RCV002483370 ; RCV004553183
• dbSNP Id: rs1555613934
• gnomAD v4: 17-31227295-T-C
• MyVariant Identifiers: chr17:g.29554313T>C (hg19) ; chr17:g.31227295T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31227295T>C , CM000679.2:g.31227295T>C	GRCh38
NC_000017.10:g.29554313T>C , CM000679.1:g.29554313T>C	GRCh37
NC_000017.9:g.26578439T>C	NCBI36
NG_009018.1:g.137319T>C , LRG_214:g.137319T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.2370+4T>C	ENSP00000512431.1:n.2370+4T>C
ENST00000691014.1:c.2355+4T>C	ENSP00000510595.1:n.2355+4T>C
ENST00000358273.9:c.2325+4T>C MANE Select	ENSP00000351015.4:n.2325+4T>C
ENST00000356175.7:c.2325+4T>C	ENSP00000348498.3:n.2325+4T>C
ENST00000358273.8:c.2325+4T>C	ENSP00000351015.4:n.2325+4T>C
ENST00000456735.6:c.1323+4T>C	ENSP00000389907.2:n.1323+4T>C
ENST00000493220.5:n.492+4T>C
ENST00000495910.6:c.2100+4T>C
ENST00000579081.5:c.2427+4T>C	ENSP00000462408.1:n.2427+4T>C
NM_000267.3:c.2325+4T>C , LRG_214t1:c.2325+4T>C	NP_000258.1:n.2325+4T>C
NM_001042492.2:c.2325+4T>C , LRG_214t2:c.2325+4T>C	NP_001035957.1:n.2325+4T>C
XM_005257983.1:c.2325+4T>C	XP_005258040.1:n.2325+4T>C
XM_005257984.1:c.2325+4T>C	XP_005258041.1:n.2325+4T>C
XM_006721922.1:c.2355+4T>C	XP_006721985.1:n.2355+4T>C
XM_006721923.2:c.2316+4T>C	XP_006721986.1:n.2316+4T>C
XM_006721924.1:c.2355+4T>C	XP_006721987.1:n.2355+4T>C
XM_006721925.1:c.2355+4T>C	XP_006721988.1:n.2355+4T>C
XM_006721926.2:c.2355+4T>C	XP_006721989.1:n.2355+4T>C
XM_006721927.1:c.2355+4T>C	XP_006721990.1:n.2355+4T>C
XM_006721928.2:c.2355+4T>C	XP_006721991.1:n.2355+4T>C
XM_011524852.1:c.2352+4T>C	XP_011523154.1:n.2352+4T>C
XM_011524853.1:c.2316+4T>C	XP_011523155.1:n.2316+4T>C
XM_011524854.1:c.2316+4T>C	XP_011523156.1:n.2316+4T>C
XM_011524855.1:c.2316+4T>C	XP_011523157.1:n.2316+4T>C
XM_011524856.1:c.2316+4T>C	XP_011523158.1:n.2316+4T>C
XM_011524857.1:c.2355+4T>C	XP_011523159.1:n.2355+4T>C
NM_001042492.3:c.2325+4T>C MANE Select	NP_001035957.1:n.2325+4T>C