Canonical Allele Identifier: CA399003981

Gene: NF1

Linked Data

• MyVariant Identifiers: chr17:g.29550469A>C (hg19) ; chr17:g.31223451A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31223451A>C , CM000679.2:g.31223451A>C	GRCh38
NC_000017.10:g.29550469A>C , CM000679.1:g.29550469A>C	GRCh37
NC_000017.9:g.26574595A>C	NCBI36
NG_009018.1:g.133475A>C , LRG_214:g.133475A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.1774A>C	ENSP00000512431.1:p.Met592Leu
ENST00000691014.1:c.1759A>C	ENSP00000510595.1:p.Met587Leu
ENST00000358273.9:c.1729A>C MANE Select	ENSP00000351015.4:p.Met577Leu
ENST00000356175.7:c.1729A>C	ENSP00000348498.3:p.Met577Leu
ENST00000358273.8:c.1729A>C	ENSP00000351015.4:p.Met577Leu
ENST00000456735.6:c.727A>C	ENSP00000389907.2:p.Met243Leu
ENST00000495910.6:c.1504A>C
ENST00000579081.5:c.1831A>C	ENSP00000462408.1:p.Met611Leu
NM_000267.3:c.1729A>C , LRG_214t1:c.1729A>C	NP_000258.1:p.Met577Leu
NM_001042492.2:c.1729A>C , LRG_214t2:c.1729A>C	NP_001035957.1:p.Met577Leu
XM_005257983.1:c.1729A>C	XP_005258040.1:p.Met577Leu
XM_005257984.1:c.1729A>C	XP_005258041.1:p.Met577Leu
XM_006721922.1:c.1759A>C	XP_006721985.1:p.Met587Leu
XM_006721923.2:c.1720A>C	XP_006721986.1:p.Met574Leu
XM_006721924.1:c.1759A>C	XP_006721987.1:p.Met587Leu
XM_006721925.1:c.1759A>C	XP_006721988.1:p.Met587Leu
XM_006721926.2:c.1759A>C	XP_006721989.1:p.Met587Leu
XM_006721927.1:c.1759A>C	XP_006721990.1:p.Met587Leu
XM_006721928.2:c.1759A>C	XP_006721991.1:p.Met587Leu
XM_011524852.1:c.1759A>C	XP_011523154.1:p.Met587Leu
XM_011524853.1:c.1720A>C	XP_011523155.1:p.Met574Leu
XM_011524854.1:c.1720A>C	XP_011523156.1:p.Met574Leu
XM_011524855.1:c.1720A>C	XP_011523157.1:p.Met574Leu
XM_011524856.1:c.1720A>C	XP_011523158.1:p.Met574Leu
XM_011524857.1:c.1759A>C	XP_011523159.1:p.Met587Leu
NM_001042492.3:c.1729A>C MANE Select	NP_001035957.1:p.Met577Leu