Canonical Allele Identifier: CA982966167
Gene: NF1 HGNC NCBI

Linked Data

dbSNP Id: rs1911533917

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31095209C>A , CM000679.2:g.31095209C>A GRCh38
NC_000017.10:g.29422227C>A , CM000679.1:g.29422227C>A GRCh37
NC_000017.9:g.26446353C>A NCBI36
NG_009018.1:g.5233C>A , LRG_214:g.5233C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696138.1:c.-101C>A ENSP00000512431.1:n.-101C>A
ENST00000691014.1:c.-101C>A ENSP00000510595.1:n.-101C>A
ENST00000358273.9:c.-101C>A MANE Select ENSP00000351015.4:n.-101C>A
ENST00000356175.7:c.-101C>A ENSP00000348498.3:n.-101C>A
ENST00000358273.8:c.-101C>A ENSP00000351015.4:n.-101C>A
ENST00000431387.8:c.-101C>A ENSP00000412921.4:n.-101C>A
ENST00000487476.5:n.283C>A
ENST00000579081.5:c.2C>A ENSP00000462408.1:p.Ser1Tyr
NM_000267.3:c.-101C>A , LRG_214t1:c.-101C>A NP_000258.1:n.-101C>A
NM_001042492.2:c.-101C>A , LRG_214t2:c.-101C>A NP_001035957.1:n.-101C>A
NM_001128147.2:c.-101C>A NP_001121619.1:n.-101C>A
XM_005257983.1:c.-101C>A XP_005258040.1:n.-101C>A
XM_005257984.1:c.-101C>A XP_005258041.1:n.-101C>A
XM_006721922.1:c.-101C>A XP_006721985.1:n.-101C>A
XM_006721923.2:c.21+23160C>A XP_006721986.1:n.21+23160C>A
XM_006721924.1:c.-101C>A XP_006721987.1:n.-101C>A
XM_006721925.1:c.-101C>A XP_006721988.1:n.-101C>A
XM_006721926.2:c.-101C>A XP_006721989.1:n.-101C>A
XM_006721927.1:c.-101C>A XP_006721990.1:n.-101C>A
XM_006721928.2:c.-101C>A XP_006721991.1:n.-101C>A
XM_011524852.1:c.-101C>A XP_011523154.1:n.-101C>A
XM_011524853.1:c.21+23160C>A XP_011523155.1:n.21+23160C>A
XM_011524854.1:c.21+23160C>A XP_011523156.1:n.21+23160C>A
XM_011524855.1:c.21+23160C>A XP_011523157.1:n.21+23160C>A
XM_011524856.1:c.21+23160C>A XP_011523158.1:n.21+23160C>A
XM_011524857.1:c.-101C>A XP_011523159.1:n.-101C>A
NM_001042492.3:c.-101C>A MANE Select NP_001035957.1:n.-101C>A
NM_001128147.3:c.-101C>A NP_001121619.1:n.-101C>A