Canonical Allele Identifier: CA1170551368

Gene: NFIA

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.61154824A>T , CM000663.2:g.61154824A>T	GRCh38
NC_000001.10:g.61620496A>T , CM000663.1:g.61620496A>T	GRCh37
NC_000001.9:g.61393084A>T	NCBI36
NG_011787.1:g.82551A>T
NG_011787.2:g.82551A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482020.2:c.559+66144A>T	ENSP00000474806.2:n.559+66144A>T
ENST00000699964.1:c.535+66144A>T	ENSP00000514720.1:n.535+66144A>T
ENST00000699965.1:c.559+66144A>T	ENSP00000514721.1:n.559+66144A>T
ENST00000699966.1:c.559+66144A>T	ENSP00000514722.1:n.559+66144A>T
ENST00000699967.1:c.559+66144A>T	ENSP00000514723.1:n.559+66144A>T
ENST00000699986.1:c.559+66144A>T	ENSP00000514739.1:n.559+66144A>T
ENST00000699987.1:c.559+66144A>T	ENSP00000514740.1:n.559+66144A>T
ENST00000699993.1:c.559+66144A>T	ENSP00000514743.1:n.559+66144A>T
ENST00000403491.8:c.559+66144A>T MANE Select	ENSP00000384523.3:n.559+66144A>T
ENST00000662015.1:c.*129+42481A>T	ENSP00000499312.1:n.*129+42481A>T
ENST00000664149.1:c.559+66144A>T	ENSP00000499651.1:n.559+66144A>T
ENST00000664495.1:c.*651+66144A>T	ENSP00000499306.1:n.*651+66144A>T
ENST00000670151.1:c.559+66144A>T	ENSP00000499729.1:n.559+66144A>T
ENST00000371184.6:c.559+66144A>T	ENSP00000360226.1:n.559+66144A>T
ENST00000371185.6:c.559+66144A>T	ENSP00000360227.1:n.559+66144A>T
ENST00000371187.7:c.559+66144A>T	ENSP00000360229.3:n.559+66144A>T
ENST00000371189.8:c.694+66144A>T	ENSP00000360231.3:n.694+66144A>T
ENST00000371191.5:c.628+66144A>T	ENSP00000360233.1:n.628+66144A>T
ENST00000403491.7:c.559+66144A>T	ENSP00000384523.3:n.559+66144A>T
ENST00000407417.7:c.535+66144A>T	ENSP00000384680.2:n.535+66144A>T
ENST00000476646.5:c.418+66144A>T	ENSP00000474461.1:n.418+66144A>T
ENST00000479364.1:n.149+72909A>T
ENST00000485903.6:c.559+66144A>T	ENSP00000419785.2:n.559+66144A>T
NM_001134673.3:c.559+66144A>T	NP_001128145.1:n.559+66144A>T
NM_001145511.1:c.535+66144A>T	NP_001138983.1:n.535+66144A>T
NM_001145512.1:c.694+66144A>T	NP_001138984.1:n.694+66144A>T
NM_005595.4:c.559+66144A>T	NP_005586.1:n.559+66144A>T
XM_011541512.1:c.559+66144A>T	XP_011539814.1:n.559+66144A>T
XM_011541513.1:c.559+66144A>T	XP_011539815.1:n.559+66144A>T
XM_011541514.1:c.535+66144A>T	XP_011539816.1:n.535+66144A>T
XM_011541515.1:c.559+66144A>T	XP_011539817.1:n.559+66144A>T
XM_011541512.3:c.559+66144A>T	XP_011539814.1:n.559+66144A>T
XM_011541514.3:c.535+66144A>T	XP_011539816.1:n.535+66144A>T
XM_011541515.3:c.559+66144A>T	XP_011539817.1:n.559+66144A>T
XM_017001362.2:c.535+66144A>T	XP_016856851.1:n.535+66144A>T
NM_001134673.4:c.559+66144A>T MANE Select	NP_001128145.1:n.559+66144A>T
NM_001145511.2:c.535+66144A>T	NP_001138983.1:n.535+66144A>T
NM_001145512.2:c.694+66144A>T	NP_001138984.1:n.694+66144A>T
NM_005595.5:c.559+66144A>T	NP_005586.1:n.559+66144A>T