Canonical Allele Identifier: CA289377010
Gene: NF1 HGNC NCBI

Linked Data

dbSNP Id: rs1030894122

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31325756T>C , CM000679.2:g.31325756T>C GRCh38
NC_000017.10:g.29652774T>C , CM000679.1:g.29652774T>C GRCh37
NC_000017.9:g.26676900T>C NCBI36
NG_009018.1:g.235780T>C , LRG_214:g.235780T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000581113.7:c.1024-64T>C ENSP00000492721.2:n.1024-64T>C
ENST00000696138.1:c.4818-64T>C ENSP00000512431.1:n.4818-64T>C
ENST00000684826.1:c.-601-64T>C ENSP00000509994.1:n.-601-64T>C
ENST00000687027.1:c.-668-64T>C ENSP00000508715.1:n.-668-64T>C
ENST00000687863.1:n.1481-64T>C
ENST00000691014.1:c.4866-64T>C ENSP00000510595.1:n.4866-64T>C
ENST00000693617.1:c.-601-64T>C ENSP00000510031.1:n.-601-64T>C
ENST00000358273.9:c.4836-64T>C MANE Select ENSP00000351015.4:n.4836-64T>C
ENST00000356175.7:c.4773-64T>C ENSP00000348498.3:n.4773-64T>C
ENST00000358273.8:c.4836-64T>C ENSP00000351015.4:n.4836-64T>C
ENST00000456735.6:c.3771-64T>C ENSP00000389907.2:n.3771-64T>C
ENST00000493220.5:n.3309-64T>C
ENST00000579081.5:c.4972-64T>C ENSP00000462408.1:n.4972-64T>C
ENST00000581113.6:n.153-64T>C
NM_000267.3:c.4773-64T>C , LRG_214t1:c.4773-64T>C NP_000258.1:n.4773-64T>C
NM_001042492.2:c.4836-64T>C , LRG_214t2:c.4836-64T>C NP_001035957.1:n.4836-64T>C
XM_005257983.1:c.4836-64T>C XP_005258040.1:n.4836-64T>C
XM_005257984.1:c.4773-64T>C XP_005258041.1:n.4773-64T>C
XM_006721922.1:c.4866-64T>C XP_006721985.1:n.4866-64T>C
XM_006721923.2:c.4827-64T>C XP_006721986.1:n.4827-64T>C
XM_006721924.1:c.4866-64T>C XP_006721987.1:n.4866-64T>C
XM_006721925.1:c.4803-64T>C XP_006721988.1:n.4803-64T>C
XM_006721926.2:c.4866-64T>C XP_006721989.1:n.4866-64T>C
XM_006721927.1:c.4866-64T>C XP_006721990.1:n.4866-64T>C
XM_011524852.1:c.4863-64T>C XP_011523154.1:n.4863-64T>C
XM_011524853.1:c.4827-64T>C XP_011523155.1:n.4827-64T>C
XM_011524854.1:c.4827-64T>C XP_011523156.1:n.4827-64T>C
XM_011524855.1:c.4827-64T>C XP_011523157.1:n.4827-64T>C
XM_011524856.1:c.4827-64T>C XP_011523158.1:n.4827-64T>C
XM_011524857.1:c.4866-64T>C XP_011523159.1:n.4866-64T>C
NM_001042492.3:c.4836-64T>C MANE Select NP_001035957.1:n.4836-64T>C