Canonical Allele Identifier: CA398984667

Gene: NF1

Linked Data

• ClinVar Variation Id: 481882
• ClinVar RCV Id: RCV000659962 ; RCV001837995 ; RCV002316596
• dbSNP Id: rs1555607073
• MyVariant Identifiers: chr17:g.29496913C>T (hg19) ; chr17:g.31169895C>T (hg38)
• PubMed: PMID:17514731 ; PMID:25525159

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31169895C>T , CM000679.2:g.31169895C>T	GRCh38
NC_000017.10:g.29496913C>T , CM000679.1:g.29496913C>T	GRCh37
NC_000017.9:g.26521039C>T	NCBI36
NG_009018.1:g.79919C>T , LRG_214:g.79919C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.484C>T	ENSP00000512431.1:p.Gln162Ter
ENST00000691014.1:c.484C>T	ENSP00000510595.1:p.Gln162Ter
ENST00000358273.9:c.484C>T MANE Select	ENSP00000351015.4:p.Gln162Ter
ENST00000490416.2:c.166+6519C>T	ENSP00000491431.1:n.166+6519C>T
ENST00000356175.7:c.484C>T	ENSP00000348498.3:p.Gln162Ter
ENST00000358273.8:c.484C>T	ENSP00000351015.4:p.Gln162Ter
ENST00000431387.8:c.484C>T	ENSP00000412921.4:p.Gln162Ter
ENST00000487476.5:n.867C>T
ENST00000489712.6:c.283C>T	ENSP00000467284.1:p.Gln95Ter
ENST00000490416.1:n.220+6519C>T
ENST00000495910.6:c.361+6519C>T
ENST00000579081.5:c.586C>T	ENSP00000462408.1:p.Gln196Ter
NM_000267.3:c.484C>T , LRG_214t1:c.484C>T	NP_000258.1:p.Gln162Ter
NM_001042492.2:c.484C>T , LRG_214t2:c.484C>T	NP_001035957.1:p.Gln162Ter
NM_001128147.2:c.484C>T	NP_001121619.1:p.Gln162Ter
XM_005257983.1:c.484C>T	XP_005258040.1:p.Gln162Ter
XM_005257984.1:c.484C>T	XP_005258041.1:p.Gln162Ter
XM_006721922.1:c.484C>T	XP_006721985.1:p.Gln162Ter
XM_006721923.2:c.445C>T	XP_006721986.1:p.Gln149Ter
XM_006721924.1:c.484C>T	XP_006721987.1:p.Gln162Ter
XM_006721925.1:c.484C>T	XP_006721988.1:p.Gln162Ter
XM_006721926.2:c.484C>T	XP_006721989.1:p.Gln162Ter
XM_006721927.1:c.484C>T	XP_006721990.1:p.Gln162Ter
XM_006721928.2:c.484C>T	XP_006721991.1:p.Gln162Ter
XM_011524852.1:c.484C>T	XP_011523154.1:p.Gln162Ter
XM_011524853.1:c.445C>T	XP_011523155.1:p.Gln149Ter
XM_011524854.1:c.445C>T	XP_011523156.1:p.Gln149Ter
XM_011524855.1:c.445C>T	XP_011523157.1:p.Gln149Ter
XM_011524856.1:c.445C>T	XP_011523158.1:p.Gln149Ter
XM_011524857.1:c.484C>T	XP_011523159.1:p.Gln162Ter
NM_001042492.3:c.484C>T MANE Select	NP_001035957.1:p.Gln162Ter
NM_001128147.3:c.484C>T	NP_001121619.1:p.Gln162Ter