Canonical Allele Identifier: CA399014261

Gene: NF1

Linked Data

• dbSNP Id: rs1597845918
• MyVariant Identifiers: chr17:g.29665732G>C (hg19) ; chr17:g.31338714G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31338714G>C , CM000679.2:g.31338714G>C	GRCh38
NC_000017.10:g.29665732G>C , CM000679.1:g.29665732G>C	GRCh37
NC_000017.9:g.26689858G>C	NCBI36
NG_009018.1:g.248738G>C , LRG_214:g.248738G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696138.1:c.6812G>C	ENSP00000512431.1:p.Ser2271Thr
ENST00000684826.1:c.1394G>C	ENSP00000509994.1:p.Ser465Thr
ENST00000684998.1:n.2652G>C
ENST00000687027.1:c.986G>C	ENSP00000508715.1:p.Ser329Thr
ENST00000687863.1:n.3475G>C
ENST00000691014.1:c.6860G>C	ENSP00000510595.1:p.Ser2287Thr
ENST00000693617.1:c.1394G>C	ENSP00000510031.1:p.Ser465Thr
ENST00000358273.9:c.6830G>C MANE Select	ENSP00000351015.4:p.Ser2277Thr
ENST00000356175.7:c.6767G>C	ENSP00000348498.3:p.Ser2256Thr
ENST00000358273.8:c.6830G>C	ENSP00000351015.4:p.Ser2277Thr
ENST00000456735.6:c.5765G>C	ENSP00000389907.2:p.Ser1922Thr
ENST00000471572.6:c.213G>C
ENST00000579081.5:c.6966G>C	ENSP00000462408.1:n.6966G>C
ENST00000581790.5:c.64+834G>C
ENST00000584328.1:n.244G>C
NM_000267.3:c.6767G>C , LRG_214t1:c.6767G>C	NP_000258.1:p.Ser2256Thr
NM_001042492.2:c.6830G>C , LRG_214t2:c.6830G>C	NP_001035957.1:p.Ser2277Thr
XM_005257983.1:c.6830G>C	XP_005258040.1:p.Ser2277Thr
XM_005257984.1:c.6767G>C	XP_005258041.1:p.Ser2256Thr
XM_006721922.1:c.6860G>C	XP_006721985.1:p.Ser2287Thr
XM_006721923.2:c.6821G>C	XP_006721986.1:p.Ser2274Thr
XM_006721924.1:c.6860G>C	XP_006721987.1:p.Ser2287Thr
XM_006721925.1:c.6797G>C	XP_006721988.1:p.Ser2266Thr
XM_006721926.2:c.6860G>C	XP_006721989.1:p.Ser2287Thr
XM_006721927.1:c.6860G>C	XP_006721990.1:p.Ser2287Thr
XM_011524852.1:c.6857G>C	XP_011523154.1:p.Ser2286Thr
XM_011524853.1:c.6821G>C	XP_011523155.1:p.Ser2274Thr
XM_011524854.1:c.6821G>C	XP_011523156.1:p.Ser2274Thr
XM_011524855.1:c.6821G>C	XP_011523157.1:p.Ser2274Thr
XM_011524856.1:c.6821G>C	XP_011523158.1:p.Ser2274Thr
XM_011524857.1:c.6860G>C	XP_011523159.1:p.Ser2287Thr
NM_001042492.3:c.6830G>C MANE Select	NP_001035957.1:p.Ser2277Thr