Canonical Allele Identifier: CA2171411489

Gene: FSIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.39618230A= , CM000677.2:g.39618230A=	GRCh38
NC_000015.9:g.39910431A= , CM000677.1:g.39910431A=	GRCh37
NC_000015.8:g.37697723A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_152597.5:c.1204T= MANE Select	NP_689810.3:p.Cys402=
ENST00000350221.4:c.1204T= MANE Select	ENSP00000280236.3:p.Cys402=
NM_001324338.1:c.1204T=	NP_001311267.1:p.Cys402=
NM_001324338.2:c.1204T=	NP_001311267.1:p.Cys402=
NM_152597.4:c.1204T=	NP_689810.3:p.Cys402=
ENST00000350221.3:c.1204T=	ENSP00000280236.3:p.Cys402=
ENST00000642527.1:c.14T=
XM_005254208.2:c.1204T=	XP_005254265.1:p.Cys402=
XM_011521305.1:c.1204T=	XP_011519607.1:p.Cys402=
XM_011521305.3:c.1204T=	XP_011519607.1:p.Cys402=
XM_011521306.1:c.1204T=	XP_011519608.1:p.Cys402=
XM_011521306.2:c.1204T=	XP_011519608.1:p.Cys402=
XM_011521308.1:c.1200T=	XP_011519610.1:p.His400=
XM_011521311.1:c.574T=	XP_011519613.1:p.Cys192=
XM_011521311.3:c.574T=	XP_011519613.1:p.Cys192=
XM_017021972.2:c.574T=	XP_016877461.1:p.Cys192=