Canonical Allele Identifier: CA398986396

Gene: NF1

Linked Data

• MyVariant Identifiers: chr17:g.29556976A>C (hg19) ; chr17:g.31229958A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31229958A>C , CM000679.2:g.31229958A>C	GRCh38
NC_000017.10:g.29556976A>C , CM000679.1:g.29556976A>C	GRCh37
NC_000017.9:g.26581102A>C	NCBI36
NG_009018.1:g.139982A>C , LRG_214:g.139982A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.3019A>C	ENSP00000512431.1:p.Met1007Leu
ENST00000696139.1:c.319A>C	ENSP00000512432.1:p.Met107Leu
ENST00000691014.1:c.3004A>C	ENSP00000510595.1:p.Met1002Leu
ENST00000358273.9:c.2974A>C MANE Select	ENSP00000351015.4:p.Met992Leu
ENST00000356175.7:c.2974A>C	ENSP00000348498.3:p.Met992Leu
ENST00000358273.8:c.2974A>C	ENSP00000351015.4:p.Met992Leu
ENST00000456735.6:c.1972A>C	ENSP00000389907.2:p.Met658Leu
ENST00000493220.5:n.1510A>C
ENST00000495910.6:c.2749A>C
ENST00000579081.5:c.3076A>C	ENSP00000462408.1:p.Met1026Leu
NM_000267.3:c.2974A>C , LRG_214t1:c.2974A>C	NP_000258.1:p.Met992Leu
NM_001042492.2:c.2974A>C , LRG_214t2:c.2974A>C	NP_001035957.1:p.Met992Leu
XM_005257983.1:c.2974A>C	XP_005258040.1:p.Met992Leu
XM_005257984.1:c.2974A>C	XP_005258041.1:p.Met992Leu
XM_006721922.1:c.3004A>C	XP_006721985.1:p.Met1002Leu
XM_006721923.2:c.2965A>C	XP_006721986.1:p.Met989Leu
XM_006721924.1:c.3004A>C	XP_006721987.1:p.Met1002Leu
XM_006721925.1:c.3004A>C	XP_006721988.1:p.Met1002Leu
XM_006721926.2:c.3004A>C	XP_006721989.1:p.Met1002Leu
XM_006721927.1:c.3004A>C	XP_006721990.1:p.Met1002Leu
XM_006721928.2:c.3004A>C	XP_006721991.1:p.Met1002Leu
XM_011524852.1:c.3001A>C	XP_011523154.1:p.Met1001Leu
XM_011524853.1:c.2965A>C	XP_011523155.1:p.Met989Leu
XM_011524854.1:c.2965A>C	XP_011523156.1:p.Met989Leu
XM_011524855.1:c.2965A>C	XP_011523157.1:p.Met989Leu
XM_011524856.1:c.2965A>C	XP_011523158.1:p.Met989Leu
XM_011524857.1:c.3004A>C	XP_011523159.1:p.Met1002Leu
NM_001042492.3:c.2974A>C MANE Select	NP_001035957.1:p.Met992Leu