Canonical Allele Identifier: CA737616677

Gene: NFIA

Linked Data

• dbSNP Id: rs6691768
• gnomAD v3: 1-61326191-G-C
• gnomAD v4: 1-61326191-G-C
• MyVariant Identifiers: chr1:g.61791863G>C (hg19) ; chr1:g.61326191G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.61326191G>C , CM000663.2:g.61326191G>C	GRCh38
NC_000001.10:g.61791863G>C , CM000663.1:g.61791863G>C	GRCh37
NC_000001.9:g.61564451G>C	NCBI36
NG_011787.1:g.253918G>C
NG_011787.2:g.253918G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000482020.2:c.626-6321G>C	ENSP00000474806.2:n.626-6321G>C
ENST00000699964.1:c.602-6321G>C	ENSP00000514720.1:n.602-6321G>C
ENST00000699965.1:c.626-6321G>C	ENSP00000514721.1:n.626-6321G>C
ENST00000699966.1:c.626-6321G>C	ENSP00000514722.1:n.626-6321G>C
ENST00000699967.1:c.626-6321G>C	ENSP00000514723.1:n.626-6321G>C
ENST00000699968.1:c.101-6321G>C	ENSP00000514724.1:n.101-6321G>C
ENST00000699986.1:c.560-6321G>C	ENSP00000514739.1:n.560-6321G>C
ENST00000699987.1:c.626-2251G>C	ENSP00000514740.1:n.626-2251G>C
ENST00000699993.1:c.626-6321G>C	ENSP00000514743.1:n.626-6321G>C
ENST00000403491.8:c.626-6321G>C MANE Select	ENSP00000384523.3:n.626-6321G>C
ENST00000655770.1:c.-143-6321G>C	ENSP00000499326.1:n.-143-6321G>C
ENST00000657234.1:c.-143-6321G>C	ENSP00000499693.1:n.-143-6321G>C
ENST00000662015.1:c.*196-6321G>C	ENSP00000499312.1:n.*196-6321G>C
ENST00000663597.1:c.-143-6321G>C	ENSP00000499597.1:n.-143-6321G>C
ENST00000664149.1:c.626-6321G>C	ENSP00000499651.1:n.626-6321G>C
ENST00000664495.1:c.*718-6321G>C	ENSP00000499306.1:n.*718-6321G>C
ENST00000670151.1:c.626-6321G>C	ENSP00000499729.1:n.626-6321G>C
ENST00000371184.6:c.560-57046G>C	ENSP00000360226.1:n.560-57046G>C
ENST00000371185.6:c.560-6321G>C	ENSP00000360227.1:n.560-6321G>C
ENST00000371187.7:c.626-6321G>C	ENSP00000360229.3:n.626-6321G>C
ENST00000371189.8:c.761-6321G>C	ENSP00000360231.3:n.761-6321G>C
ENST00000371191.5:c.695-6321G>C	ENSP00000360233.1:n.695-6321G>C
ENST00000403491.7:c.626-6321G>C	ENSP00000384523.3:n.626-6321G>C
ENST00000407417.7:c.602-6321G>C	ENSP00000384680.2:n.602-6321G>C
ENST00000476646.5:c.485-6321G>C	ENSP00000474461.1:n.485-6321G>C
ENST00000479364.1:n.216-6321G>C
ENST00000485903.6:c.626-6321G>C	ENSP00000419785.2:n.626-6321G>C
NM_001134673.3:c.626-6321G>C	NP_001128145.1:n.626-6321G>C
NM_001145511.1:c.602-6321G>C	NP_001138983.1:n.602-6321G>C
NM_001145512.1:c.761-6321G>C	NP_001138984.1:n.761-6321G>C
NM_005595.4:c.626-6321G>C	NP_005586.1:n.626-6321G>C
XM_011541512.1:c.626-6321G>C	XP_011539814.1:n.626-6321G>C
XM_011541513.1:c.626-6321G>C	XP_011539815.1:n.626-6321G>C
XM_011541514.1:c.602-6321G>C	XP_011539816.1:n.602-6321G>C
XM_011541515.1:c.626-6321G>C	XP_011539817.1:n.626-6321G>C
XM_011541512.3:c.626-6321G>C	XP_011539814.1:n.626-6321G>C
XM_011541514.3:c.602-6321G>C	XP_011539816.1:n.602-6321G>C
XM_011541515.3:c.626-6321G>C	XP_011539817.1:n.626-6321G>C
XM_017001362.2:c.602-6321G>C	XP_016856851.1:n.602-6321G>C
XM_017001363.1:c.-143-6321G>C	XP_016856852.1:n.-143-6321G>C
NM_001134673.4:c.626-6321G>C MANE Select	NP_001128145.1:n.626-6321G>C
NM_001145511.2:c.602-6321G>C	NP_001138983.1:n.602-6321G>C
NM_001145512.2:c.761-6321G>C	NP_001138984.1:n.761-6321G>C
NM_005595.5:c.626-6321G>C	NP_005586.1:n.626-6321G>C