Canonical Allele Identifier: CA10580232

Gene: NF1

Linked Data

• ClinVar Variation Id: 229665
• ClinVar RCV Id: RCV000213679 ; RCV000681361 ; RCV001088968
• dbSNP Id: rs876658128
• MyVariant Identifiers: chr17:g.29550474T>C (hg19) ; chr17:g.31223456T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31223456T>C , CM000679.2:g.31223456T>C	GRCh38
NC_000017.10:g.29550474T>C , CM000679.1:g.29550474T>C	GRCh37
NC_000017.9:g.26574600T>C	NCBI36
NG_009018.1:g.133480T>C , LRG_214:g.133480T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.1779T>C	ENSP00000512431.1:p.Leu593=
ENST00000691014.1:c.1764T>C	ENSP00000510595.1:p.Leu588=
ENST00000358273.9:c.1734T>C MANE Select	ENSP00000351015.4:p.Leu578=
ENST00000356175.7:c.1734T>C	ENSP00000348498.3:p.Leu578=
ENST00000358273.8:c.1734T>C	ENSP00000351015.4:p.Leu578=
ENST00000456735.6:c.732T>C	ENSP00000389907.2:p.Leu244=
ENST00000495910.6:c.1509T>C
ENST00000579081.5:c.1836T>C	ENSP00000462408.1:p.Leu612=
NM_000267.3:c.1734T>C , LRG_214t1:c.1734T>C	NP_000258.1:p.Leu578=
NM_001042492.2:c.1734T>C , LRG_214t2:c.1734T>C	NP_001035957.1:p.Leu578=
XM_005257983.1:c.1734T>C	XP_005258040.1:p.Leu578=
XM_005257984.1:c.1734T>C	XP_005258041.1:p.Leu578=
XM_006721922.1:c.1764T>C	XP_006721985.1:p.Leu588=
XM_006721923.2:c.1725T>C	XP_006721986.1:p.Leu575=
XM_006721924.1:c.1764T>C	XP_006721987.1:p.Leu588=
XM_006721925.1:c.1764T>C	XP_006721988.1:p.Leu588=
XM_006721926.2:c.1764T>C	XP_006721989.1:p.Leu588=
XM_006721927.1:c.1764T>C	XP_006721990.1:p.Leu588=
XM_006721928.2:c.1764T>C	XP_006721991.1:p.Leu588=
XM_011524852.1:c.1764T>C	XP_011523154.1:p.Leu588=
XM_011524853.1:c.1725T>C	XP_011523155.1:p.Leu575=
XM_011524854.1:c.1725T>C	XP_011523156.1:p.Leu575=
XM_011524855.1:c.1725T>C	XP_011523157.1:p.Leu575=
XM_011524856.1:c.1725T>C	XP_011523158.1:p.Leu575=
XM_011524857.1:c.1764T>C	XP_011523159.1:p.Leu588=
NM_001042492.3:c.1734T>C MANE Select	NP_001035957.1:p.Leu578=