Canonical Allele Identifier: CA2499214344

Gene: NCF2 SMG7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183564051G>A , CM000663.2:g.183564051G>A	GRCh38
NC_000001.10:g.183533186G>A , CM000663.1:g.183533186G>A	GRCh37
NC_000001.9:g.181799809G>A	NCBI36
NG_007267.1:g.31531C>T , LRG_88:g.31531C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000433.4:c.1001-21C>T (NCF2) MANE Select	NP_000424.2:n.1001-21C>T
ENST00000367535.8:c.1001-21C>T (NCF2) MANE Select	ENSP00000356505.4:n.1001-21C>T
NM_000433.3:c.1001-21C>T , LRG_88t1:c.1001-21C>T (NCF2)	NP_000424.2:n.1001-21C>T
NM_001127651.2:c.1001-21C>T (NCF2)	NP_001121123.1:n.1001-21C>T
NM_001127651.3:c.1001-21C>T (NCF2)	NP_001121123.1:n.1001-21C>T
NM_001190789.1:c.758-21C>T (NCF2)	NP_001177718.1:n.758-21C>T
NM_001190789.2:c.758-21C>T (NCF2)	NP_001177718.1:n.758-21C>T
NM_001190794.1:c.866-21C>T (NCF2)	NP_001177723.1:n.866-21C>T
NM_001190794.2:c.866-21C>T (NCF2)	NP_001177723.1:n.866-21C>T
ENST00000367535.7:c.1001-21C>T (NCF2)	ENSP00000356505.3:n.1001-21C>T
ENST00000367536.5:c.1001-21C>T (NCF2)	ENSP00000356506.1:n.1001-21C>T
ENST00000413720.5:c.866-21C>T (NCF2)	ENSP00000399294.1:n.866-21C>T
ENST00000418089.5:c.758-21C>T (NCF2)	ENSP00000407217.1:n.758-21C>T
ENST00000419402.1:c.218-21C>T (NCF2)	ENSP00000406198.1:n.218-21C>T
ENST00000420553.5:c.-47-21C>T (NCF2)	ENSP00000397228.1:n.-47-21C>T
ENST00000469280.1:n.1C>T (NCF2)
ENST00000469280.2:n.1C>T (NCF2)
ENST00000495321.1:n.233+12861G>A (SMG7)
ENST00000697329.1:n.921-21C>T (NCF2)
ENST00000697330.1:c.1001-21C>T (NCF2)	ENSP00000513258.1:n.1001-21C>T
ENST00000697351.1:c.893-21C>T (NCF2)	ENSP00000513276.1:n.893-21C>T
XM_005245207.1:c.893-21C>T (NCF2)	XP_005245264.1:n.893-21C>T
XM_011509580.1:c.1001-21C>T (NCF2)	XP_011507882.1:n.1001-21C>T
XM_011509581.1:c.1001-21C>T (NCF2)	XP_011507883.1:n.1001-21C>T
XR_921801.1:n.1063-21C>T (NCF2)