Canonical Allele Identifier: CA399010590

Gene: NF1

Linked Data

• dbSNP Id: rs2151550284
• MyVariant Identifiers: chr17:g.29661873C>T (hg19) ; chr17:g.31334855C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31334855C>T , CM000679.2:g.31334855C>T	GRCh38
NC_000017.10:g.29661873C>T , CM000679.1:g.29661873C>T	GRCh37
NC_000017.9:g.26685999C>T	NCBI36
NG_009018.1:g.244879C>T , LRG_214:g.244879C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000581113.7:c.2018C>T	ENSP00000492721.2:n.2018C>T
ENST00000696138.1:c.5812C>T	ENSP00000512431.1:p.Leu1938Phe
ENST00000684826.1:c.394C>T	ENSP00000509994.1:p.Leu132Phe
ENST00000687027.1:c.-15C>T	ENSP00000508715.1:n.-15C>T
ENST00000687863.1:n.2475C>T
ENST00000691014.1:c.5860C>T	ENSP00000510595.1:p.Leu1954Phe
ENST00000693617.1:c.394C>T	ENSP00000510031.1:p.Leu132Phe
ENST00000358273.9:c.5830C>T MANE Select	ENSP00000351015.4:p.Leu1944Phe
ENST00000356175.7:c.5767C>T	ENSP00000348498.3:p.Leu1923Phe
ENST00000358273.8:c.5830C>T	ENSP00000351015.4:p.Leu1944Phe
ENST00000456735.6:c.4765C>T	ENSP00000389907.2:p.Leu1589Phe
ENST00000479536.2:c.255C>T
ENST00000579081.5:c.5966C>T	ENSP00000462408.1:n.5966C>T
ENST00000581113.6:n.1147C>T
NM_000267.3:c.5767C>T , LRG_214t1:c.5767C>T	NP_000258.1:p.Leu1923Phe
NM_001042492.2:c.5830C>T , LRG_214t2:c.5830C>T	NP_001035957.1:p.Leu1944Phe
XM_005257983.1:c.5830C>T	XP_005258040.1:p.Leu1944Phe
XM_005257984.1:c.5767C>T	XP_005258041.1:p.Leu1923Phe
XM_006721922.1:c.5860C>T	XP_006721985.1:p.Leu1954Phe
XM_006721923.2:c.5821C>T	XP_006721986.1:p.Leu1941Phe
XM_006721924.1:c.5860C>T	XP_006721987.1:p.Leu1954Phe
XM_006721925.1:c.5797C>T	XP_006721988.1:p.Leu1933Phe
XM_006721926.2:c.5860C>T	XP_006721989.1:p.Leu1954Phe
XM_006721927.1:c.5860C>T	XP_006721990.1:p.Leu1954Phe
XM_011524852.1:c.5857C>T	XP_011523154.1:p.Leu1953Phe
XM_011524853.1:c.5821C>T	XP_011523155.1:p.Leu1941Phe
XM_011524854.1:c.5821C>T	XP_011523156.1:p.Leu1941Phe
XM_011524855.1:c.5821C>T	XP_011523157.1:p.Leu1941Phe
XM_011524856.1:c.5821C>T	XP_011523158.1:p.Leu1941Phe
XM_011524857.1:c.5860C>T	XP_011523159.1:p.Leu1954Phe
NM_001042492.3:c.5830C>T MANE Select	NP_001035957.1:p.Leu1944Phe