Canonical Allele Identifier: CA2147417590

Gene: FOS

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75280415G= , CM000676.2:g.75280415G=	GRCh38
NC_000014.8:g.75747118G= , CM000676.1:g.75747118G=	GRCh37
NC_000014.7:g.74816871G=	NCBI36
NG_029673.1:g.6638G=

Transcript Alleles

HGVS	Amino-acid Change
NM_005252.4:c.394-145G= MANE Select	NP_005243.1:n.394-145G=
ENST00000303562.9:c.394-145G= MANE Select	ENSP00000306245.4:n.394-145G=
NM_005252.3:c.394-145G=	NP_005243.1:n.394-145G=
ENST00000303562.8:c.394-145G=	ENSP00000306245.4:n.394-145G=
ENST00000535987.5:c.393+287G=	ENSP00000442268.1:n.393+287G=
ENST00000554212.5:c.365-145G=	ENSP00000452443.1:n.365-145G=
ENST00000555242.1:c.394-145G=	ENSP00000452386.1:n.394-145G=
ENST00000555347.1:c.-196G=	ENSP00000450886.1:n.-196G=
ENST00000555672.1:c.51+287G=	ENSP00000452440.1:n.51+287G=
ENST00000555686.1:c.52-145G=	ENSP00000452590.1:n.52-145G=
ENST00000557139.1:c.152-155G=	ENSP00000451786.1:n.152-155G=