Canonical Allele Identifier: CA1883419547

Gene: FCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134887245G= , CM000671.2:g.134887245G=	GRCh38
NC_000009.11:g.137779091G= , CM000671.1:g.137779091G=	GRCh37
NC_000009.10:g.136918912G=	NCBI36
NG_011649.1:g.11434G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291744.11:c.772G= MANE Select	ENSP00000291744.6:p.Ala258=
ENST00000291744.10:c.772G=	ENSP00000291744.6:p.Ala258=
ENST00000350339.3:c.658G=	ENSP00000291741.5:p.Ala220=
NM_004108.2:c.772G=	NP_004099.2:p.Ala258=
NM_015837.2:c.658G=	NP_056652.1:p.Ala220=
XM_006717015.2:c.625G=	XP_006717078.1:p.Ala209=
XM_011518392.1:c.739G=	XP_011516694.1:p.Ala247=
XM_006717015.4:c.625G=	XP_006717078.1:p.Ala209=
XM_011518392.3:c.739G=	XP_011516694.1:p.Ala247=
NM_004108.3:c.772G= MANE Select	NP_004099.2:p.Ala258=
NM_015837.3:c.658G=	NP_056652.1:p.Ala220=