Canonical Allele Identifier: CA499233561
Gene: NF1 HGNC NCBI

Linked Data

dbSNP Id: rs2151544965
MyVariant Identifiers: chr17:g.29657494T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31330476T>C , CM000679.2:g.31330476T>C GRCh38
NC_000017.10:g.29657494T>C , CM000679.1:g.29657494T>C GRCh37
NC_000017.9:g.26681620T>C NCBI36
NG_009018.1:g.240500T>C , LRG_214:g.240500T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000581113.7:c.1978T>C ENSP00000492721.2:n.1978T>C
ENST00000696138.1:c.5772T>C ENSP00000512431.1:p.Cys1924=
ENST00000684826.1:c.354T>C ENSP00000509994.1:p.Cys118=
ENST00000687027.1:c.-55T>C ENSP00000508715.1:n.-55T>C
ENST00000687863.1:n.2435T>C
ENST00000691014.1:c.5820T>C ENSP00000510595.1:p.Cys1940=
ENST00000693617.1:c.354T>C ENSP00000510031.1:p.Cys118=
ENST00000358273.9:c.5790T>C MANE Select ENSP00000351015.4:p.Cys1930=
ENST00000356175.7:c.5727T>C ENSP00000348498.3:p.Cys1909=
ENST00000358273.8:c.5790T>C ENSP00000351015.4:p.Cys1930=
ENST00000456735.6:c.4725T>C ENSP00000389907.2:p.Cys1575=
ENST00000479536.2:c.148T>C
ENST00000493220.5:n.4263T>C
ENST00000579081.5:c.5926T>C ENSP00000462408.1:n.5926T>C
ENST00000581113.6:n.1107T>C
NM_000267.3:c.5727T>C , LRG_214t1:c.5727T>C NP_000258.1:p.Cys1909=
NM_001042492.2:c.5790T>C , LRG_214t2:c.5790T>C NP_001035957.1:p.Cys1930=
XM_005257983.1:c.5790T>C XP_005258040.1:p.Cys1930=
XM_005257984.1:c.5727T>C XP_005258041.1:p.Cys1909=
XM_006721922.1:c.5820T>C XP_006721985.1:p.Cys1940=
XM_006721923.2:c.5781T>C XP_006721986.1:p.Cys1927=
XM_006721924.1:c.5820T>C XP_006721987.1:p.Cys1940=
XM_006721925.1:c.5757T>C XP_006721988.1:p.Cys1919=
XM_006721926.2:c.5820T>C XP_006721989.1:p.Cys1940=
XM_006721927.1:c.5820T>C XP_006721990.1:p.Cys1940=
XM_011524852.1:c.5817T>C XP_011523154.1:p.Cys1939=
XM_011524853.1:c.5781T>C XP_011523155.1:p.Cys1927=
XM_011524854.1:c.5781T>C XP_011523156.1:p.Cys1927=
XM_011524855.1:c.5781T>C XP_011523157.1:p.Cys1927=
XM_011524856.1:c.5781T>C XP_011523158.1:p.Cys1927=
XM_011524857.1:c.5820T>C XP_011523159.1:p.Cys1940=
NM_001042492.3:c.5790T>C MANE Select NP_001035957.1:p.Cys1930=