Canonical Allele Identifier: CA398997752

Gene: NF1

Linked Data

• gnomAD v4: 17-31201478-T-C
• MyVariant Identifiers: chr17:g.29528496T>C (hg19) ; chr17:g.31201478T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31201478T>C , CM000679.2:g.31201478T>C	GRCh38
NC_000017.10:g.29528496T>C , CM000679.1:g.29528496T>C	GRCh37
NC_000017.9:g.26552622T>C	NCBI36
NG_009018.1:g.111502T>C , LRG_214:g.111502T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.1253T>C	ENSP00000512431.1:p.Ile418Thr
ENST00000686189.1:c.668T>C	ENSP00000509682.1:p.Ile223Thr
ENST00000688507.1:n.959T>C
ENST00000691014.1:c.1253T>C	ENSP00000510595.1:p.Ile418Thr
ENST00000692326.1:n.1536T>C
ENST00000358273.9:c.1253T>C MANE Select	ENSP00000351015.4:p.Ile418Thr
ENST00000356175.7:c.1253T>C	ENSP00000348498.3:p.Ile418Thr
ENST00000358273.8:c.1253T>C	ENSP00000351015.4:p.Ile418Thr
ENST00000431387.8:c.1253T>C	ENSP00000412921.4:p.Ile418Thr
ENST00000456735.6:c.251T>C	ENSP00000389907.2:p.Ile84Thr
ENST00000487476.5:n.1636T>C
ENST00000495910.6:c.1028T>C
ENST00000579081.5:c.1355T>C	ENSP00000462408.1:p.Ile452Thr
NM_000267.3:c.1253T>C , LRG_214t1:c.1253T>C	NP_000258.1:p.Ile418Thr
NM_001042492.2:c.1253T>C , LRG_214t2:c.1253T>C	NP_001035957.1:p.Ile418Thr
NM_001128147.2:c.1253T>C	NP_001121619.1:p.Ile418Thr
XM_005257983.1:c.1253T>C	XP_005258040.1:p.Ile418Thr
XM_005257984.1:c.1253T>C	XP_005258041.1:p.Ile418Thr
XM_006721922.1:c.1253T>C	XP_006721985.1:p.Ile418Thr
XM_006721923.2:c.1214T>C	XP_006721986.1:p.Ile405Thr
XM_006721924.1:c.1253T>C	XP_006721987.1:p.Ile418Thr
XM_006721925.1:c.1253T>C	XP_006721988.1:p.Ile418Thr
XM_006721926.2:c.1253T>C	XP_006721989.1:p.Ile418Thr
XM_006721927.1:c.1253T>C	XP_006721990.1:p.Ile418Thr
XM_006721928.2:c.1253T>C	XP_006721991.1:p.Ile418Thr
XM_011524852.1:c.1253T>C	XP_011523154.1:p.Ile418Thr
XM_011524853.1:c.1214T>C	XP_011523155.1:p.Ile405Thr
XM_011524854.1:c.1214T>C	XP_011523156.1:p.Ile405Thr
XM_011524855.1:c.1214T>C	XP_011523157.1:p.Ile405Thr
XM_011524856.1:c.1214T>C	XP_011523158.1:p.Ile405Thr
XM_011524857.1:c.1253T>C	XP_011523159.1:p.Ile418Thr
NM_001042492.3:c.1253T>C MANE Select	NP_001035957.1:p.Ile418Thr
NM_001128147.3:c.1253T>C	NP_001121619.1:p.Ile418Thr