Canonical Allele Identifier: CA341836925

Gene: NGF NGF-AS1

Linked Data

• MyVariant Identifiers: chr1:g.115829151A>G (hg19) ; chr1:g.115286530A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115286530A>G , CM000663.2:g.115286530A>G	GRCh38
NC_000001.10:g.115829151A>G , CM000663.1:g.115829151A>G	GRCh37
NC_000001.9:g.115630674A>G	NCBI36
NG_007944.1:g.56707T>C , LRG_260:g.56707T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369512.3:c.266T>C (NGF) MANE Select	ENSP00000358525.2:p.Phe89Ser
ENST00000675637.2:c.266T>C (NGF)	ENSP00000502831.1:p.Phe89Ser
ENST00000676038.2:c.266T>C (NGF)	ENSP00000502380.1:p.Phe89Ser
ENST00000679806.1:c.266T>C (NGF)	ENSP00000506492.1:p.Phe89Ser
ENST00000680116.1:c.266T>C (NGF)	ENSP00000505694.1:p.Phe89Ser
ENST00000680540.1:c.266T>C (NGF)	ENSP00000506569.1:p.Phe89Ser
ENST00000680752.1:c.266T>C (NGF)	ENSP00000505558.1:p.Phe89Ser
ENST00000681124.1:c.-206T>C (NGF)	ENSP00000506364.1:n.-206T>C
ENST00000369512.2:c.266T>C (NGF)	ENSP00000358525.2:p.Phe89Ser
NM_002506.2:c.266T>C , LRG_260t1:c.266T>C (NGF)	NP_002497.2:p.Phe89Ser
XM_006710663.2:c.266T>C (NGF)	XP_006710726.1:p.Phe89Ser
XM_006710665.2:c.266T>C (NGF)	XP_006710728.1:p.Phe89Ser
XM_011541518.1:c.431T>C (NGF)	XP_011539820.1:p.Phe144Ser
NR_157569.1:n.207+3290A>G (NGF-AS1)
XM_006710663.3:c.266T>C (NGF)	XP_006710726.1:p.Phe89Ser
XM_011541518.2:c.431T>C (NGF)	XP_011539820.1:p.Phe144Ser
NM_002506.3:c.266T>C (NGF) MANE Select	NP_002497.2:p.Phe89Ser