Canonical Allele Identifier: CA10847009

Gene: NGF NGF-AS1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115333024C>T , CM000663.2:g.115333024C>T	GRCh38
NC_000001.10:g.115875645C>T , CM000663.1:g.115875645C>T	GRCh37
NC_000001.9:g.115677168C>T	NCBI36
NG_007944.1:g.10213G>A , LRG_260:g.10213G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369512.3:c.-137+5180G>A (NGF) MANE Select	ENSP00000358525.2:n.-137+5180G>A
ENST00000675637.2:c.-13+5180G>A (NGF)	ENSP00000502831.1:n.-13+5180G>A
ENST00000676038.2:c.-224+5180G>A (NGF)	ENSP00000502380.1:n.-224+5180G>A
ENST00000679806.1:c.-137+5584G>A (NGF)	ENSP00000506492.1:n.-137+5584G>A
ENST00000680116.1:c.-607+5180G>A (NGF)	ENSP00000505694.1:n.-607+5180G>A
ENST00000680752.1:c.-137+5341G>A (NGF)	ENSP00000505558.1:n.-137+5341G>A
ENST00000681124.1:c.-545+5180G>A (NGF)	ENSP00000506364.1:n.-545+5180G>A
ENST00000369512.2:c.-137+5180G>A (NGF)	ENSP00000358525.2:n.-137+5180G>A
NM_002506.2:c.-137+5180G>A , LRG_260t1:c.-137+5180G>A (NGF)	NP_002497.2:n.-137+5180G>A
XM_006710663.2:c.-13+5180G>A (NGF)	XP_006710726.1:n.-13+5180G>A
XM_006710665.2:c.-137+5341G>A (NGF)	XP_006710728.1:n.-137+5341G>A
NR_157569.1:n.208-32646C>T (NGF-AS1)
XM_006710663.3:c.-13+5180G>A (NGF)	XP_006710726.1:n.-13+5180G>A
NM_002506.3:c.-137+5180G>A (NGF) MANE Select	NP_002497.2:n.-137+5180G>A