Canonical Allele Identifier: CA499443842

Gene: NF1

Linked Data

• MyVariant Identifiers: chr17:g.29560192A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31233174A>C , CM000679.2:g.31233174A>C	GRCh38
NC_000017.10:g.29560192A>C , CM000679.1:g.29560192A>C	GRCh37
NC_000017.9:g.26584318A>C	NCBI36
NG_009018.1:g.143198A>C , LRG_214:g.143198A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.3714A>C	ENSP00000512431.1:p.Ile1238=
ENST00000696139.1:c.1014A>C	ENSP00000512432.1:p.Ile338=
ENST00000691014.1:c.3699A>C	ENSP00000510595.1:p.Ile1233=
ENST00000693210.1:n.395A>C
ENST00000358273.9:c.3669A>C MANE Select	ENSP00000351015.4:p.Ile1223=
ENST00000356175.7:c.3669A>C	ENSP00000348498.3:p.Ile1223=
ENST00000358273.8:c.3669A>C	ENSP00000351015.4:p.Ile1223=
ENST00000456735.6:c.2667A>C	ENSP00000389907.2:p.Ile889=
ENST00000466819.5:c.145A>C
ENST00000479614.1:c.145A>C
ENST00000493220.5:n.2205A>C
ENST00000495910.6:c.3444A>C
ENST00000579081.5:c.3771A>C	ENSP00000462408.1:p.Ile1257=
NM_000267.3:c.3669A>C , LRG_214t1:c.3669A>C	NP_000258.1:p.Ile1223=
NM_001042492.2:c.3669A>C , LRG_214t2:c.3669A>C	NP_001035957.1:p.Ile1223=
XM_005257983.1:c.3669A>C	XP_005258040.1:p.Ile1223=
XM_005257984.1:c.3669A>C	XP_005258041.1:p.Ile1223=
XM_006721922.1:c.3699A>C	XP_006721985.1:p.Ile1233=
XM_006721923.2:c.3660A>C	XP_006721986.1:p.Ile1220=
XM_006721924.1:c.3699A>C	XP_006721987.1:p.Ile1233=
XM_006721925.1:c.3699A>C	XP_006721988.1:p.Ile1233=
XM_006721926.2:c.3699A>C	XP_006721989.1:p.Ile1233=
XM_006721927.1:c.3699A>C	XP_006721990.1:p.Ile1233=
XM_006721928.2:c.3699A>C	XP_006721991.1:p.Ile1233=
XM_011524852.1:c.3696A>C	XP_011523154.1:p.Ile1232=
XM_011524853.1:c.3660A>C	XP_011523155.1:p.Ile1220=
XM_011524854.1:c.3660A>C	XP_011523156.1:p.Ile1220=
XM_011524855.1:c.3660A>C	XP_011523157.1:p.Ile1220=
XM_011524856.1:c.3660A>C	XP_011523158.1:p.Ile1220=
XM_011524857.1:c.3699A>C	XP_011523159.1:p.Ile1233=
NM_001042492.3:c.3669A>C MANE Select	NP_001035957.1:p.Ile1223=