Canonical Allele Identifier: CA10771952

Gene: NFIA

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.61358717G>A , CM000663.2:g.61358717G>A	GRCh38
NC_000001.10:g.61824389G>A , CM000663.1:g.61824389G>A	GRCh37
NC_000001.9:g.61596977G>A	NCBI36
NG_011787.1:g.286444G>A
NG_011787.2:g.286444G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482020.2:c.819-430G>A	ENSP00000474806.2:n.819-430G>A
ENST00000699964.1:c.795-430G>A	ENSP00000514720.1:n.795-430G>A
ENST00000699965.1:c.819-430G>A	ENSP00000514721.1:n.819-430G>A
ENST00000699966.1:c.819-430G>A	ENSP00000514722.1:n.819-430G>A
ENST00000699967.1:c.701-24520G>A	ENSP00000514723.1:n.701-24520G>A
ENST00000699968.1:c.294-430G>A	ENSP00000514724.1:n.294-430G>A
ENST00000699986.1:c.753-430G>A	ENSP00000514739.1:n.753-430G>A
ENST00000699987.1:c.942-430G>A	ENSP00000514740.1:n.942-430G>A
ENST00000699993.1:c.819-430G>A	ENSP00000514743.1:n.819-430G>A
ENST00000403491.8:c.819-430G>A MANE Select	ENSP00000384523.3:n.819-430G>A
ENST00000655770.1:c.51-430G>A	ENSP00000499326.1:n.51-430G>A
ENST00000657234.1:c.51-430G>A	ENSP00000499693.1:n.51-430G>A
ENST00000662015.1:c.*389-430G>A	ENSP00000499312.1:n.*389-430G>A
ENST00000663597.1:c.51-430G>A	ENSP00000499597.1:n.51-430G>A
ENST00000664149.1:c.819-430G>A	ENSP00000499651.1:n.819-430G>A
ENST00000664495.1:c.*911-430G>A	ENSP00000499306.1:n.*911-430G>A
ENST00000670151.1:c.819-430G>A	ENSP00000499729.1:n.819-430G>A
ENST00000371184.6:c.560-24520G>A	ENSP00000360226.1:n.560-24520G>A
ENST00000371185.6:c.753-430G>A	ENSP00000360227.1:n.753-430G>A
ENST00000371187.7:c.819-430G>A	ENSP00000360229.3:n.819-430G>A
ENST00000371189.8:c.954-430G>A	ENSP00000360231.3:n.954-430G>A
ENST00000371191.5:c.888-430G>A	ENSP00000360233.1:n.888-430G>A
ENST00000403491.7:c.819-430G>A	ENSP00000384523.3:n.819-430G>A
ENST00000407417.7:c.795-430G>A	ENSP00000384680.2:n.795-430G>A
ENST00000479364.1:n.409-430G>A
ENST00000482020.1:c.119-430G>A
ENST00000485903.6:c.819-430G>A	ENSP00000419785.2:n.819-430G>A
NM_001134673.3:c.819-430G>A	NP_001128145.1:n.819-430G>A
NM_001145511.1:c.795-430G>A	NP_001138983.1:n.795-430G>A
NM_001145512.1:c.954-430G>A	NP_001138984.1:n.954-430G>A
NM_005595.4:c.819-430G>A	NP_005586.1:n.819-430G>A
XM_011541512.1:c.819-430G>A	XP_011539814.1:n.819-430G>A
XM_011541513.1:c.819-430G>A	XP_011539815.1:n.819-430G>A
XM_011541514.1:c.795-430G>A	XP_011539816.1:n.795-430G>A
XM_011541515.1:c.819-430G>A	XP_011539817.1:n.819-430G>A
XM_011541512.3:c.819-430G>A	XP_011539814.1:n.819-430G>A
XM_011541514.3:c.795-430G>A	XP_011539816.1:n.795-430G>A
XM_011541515.3:c.819-430G>A	XP_011539817.1:n.819-430G>A
XM_017001362.2:c.795-430G>A	XP_016856851.1:n.795-430G>A
XM_017001363.1:c.51-430G>A	XP_016856852.1:n.51-430G>A
NM_001134673.4:c.819-430G>A MANE Select	NP_001128145.1:n.819-430G>A
NM_001145511.2:c.795-430G>A	NP_001138983.1:n.795-430G>A
NM_001145512.2:c.954-430G>A	NP_001138984.1:n.954-430G>A
NM_005595.5:c.819-430G>A	NP_005586.1:n.819-430G>A