Canonical Allele Identifier: CA2573153367

Gene: NF1

Linked Data

• ClinVar Variation Id: 1545655
• ClinVar RCV Id: RCV002168077
• dbSNP Id: rs2151435858

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31233226A>C , CM000679.2:g.31233226A>C	GRCh38
NC_000017.10:g.29560244A>C , CM000679.1:g.29560244A>C	GRCh37
NC_000017.9:g.26584370A>C	NCBI36
NG_009018.1:g.143250A>C , LRG_214:g.143250A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.3753+13A>C	ENSP00000512431.1:n.3753+13A>C
ENST00000696139.1:c.1053+13A>C	ENSP00000512432.1:n.1053+13A>C
ENST00000691014.1:c.3738+13A>C	ENSP00000510595.1:n.3738+13A>C
ENST00000693210.1:n.447A>C
ENST00000358273.9:c.3708+13A>C MANE Select	ENSP00000351015.4:n.3708+13A>C
ENST00000356175.7:c.3708+13A>C	ENSP00000348498.3:n.3708+13A>C
ENST00000358273.8:c.3708+13A>C	ENSP00000351015.4:n.3708+13A>C
ENST00000456735.6:c.2706+13A>C	ENSP00000389907.2:n.2706+13A>C
ENST00000466819.5:c.184+13A>C
ENST00000479614.1:c.184+13A>C
ENST00000493220.5:n.2244+13A>C
ENST00000495910.6:c.3483+13A>C
ENST00000579081.5:c.3810+13A>C	ENSP00000462408.1:n.3810+13A>C
NM_000267.3:c.3708+13A>C , LRG_214t1:c.3708+13A>C	NP_000258.1:n.3708+13A>C
NM_001042492.2:c.3708+13A>C , LRG_214t2:c.3708+13A>C	NP_001035957.1:n.3708+13A>C
XM_005257983.1:c.3708+13A>C	XP_005258040.1:n.3708+13A>C
XM_005257984.1:c.3708+13A>C	XP_005258041.1:n.3708+13A>C
XM_006721922.1:c.3738+13A>C	XP_006721985.1:n.3738+13A>C
XM_006721923.2:c.3699+13A>C	XP_006721986.1:n.3699+13A>C
XM_006721924.1:c.3738+13A>C	XP_006721987.1:n.3738+13A>C
XM_006721925.1:c.3738+13A>C	XP_006721988.1:n.3738+13A>C
XM_006721926.2:c.3738+13A>C	XP_006721989.1:n.3738+13A>C
XM_006721927.1:c.3738+13A>C	XP_006721990.1:n.3738+13A>C
XM_006721928.2:c.3738+13A>C	XP_006721991.1:n.3738+13A>C
XM_011524852.1:c.3735+13A>C	XP_011523154.1:n.3735+13A>C
XM_011524853.1:c.3699+13A>C	XP_011523155.1:n.3699+13A>C
XM_011524854.1:c.3699+13A>C	XP_011523156.1:n.3699+13A>C
XM_011524855.1:c.3699+13A>C	XP_011523157.1:n.3699+13A>C
XM_011524856.1:c.3699+13A>C	XP_011523158.1:n.3699+13A>C
XM_011524857.1:c.3738+13A>C	XP_011523159.1:n.3738+13A>C
NM_001042492.3:c.3708+13A>C MANE Select	NP_001035957.1:n.3708+13A>C