Canonical Allele Identifier: CA1140495682

Gene: GFI1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92476153T= , CM000663.2:g.92476153T=	GRCh38
NC_000001.10:g.92941710T= , CM000663.1:g.92941710T=	GRCh37
NC_000001.9:g.92714298T=	NCBI36
NG_007874.1:g.15724A= , LRG_63:g.15724A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427103.6:c.1145A=	ENSP00000399719.1:p.Asn382=
ENST00000696667.1:c.193A=	ENSP00000512792.1:p.Thr65=
ENST00000294702.6:c.1145A= MANE Select	ENSP00000294702.5:p.Asn382=
ENST00000294702.5:c.1145A=	ENSP00000294702.5:p.Asn382=
ENST00000370332.5:c.1145A=	ENSP00000359357.1:p.Asn382=
ENST00000427103.5:c.1145A=	ENSP00000399719.1:p.Asn382=
NM_001127215.1:c.1145A=	NP_001120687.1:p.Asn382=
NM_001127216.1:c.1145A=	NP_001120688.1:p.Asn382=
NM_005263.3:c.1145A= , LRG_63t1:c.1145A=	NP_005254.2:p.Asn382=
XM_005270749.3:c.1145A=	XP_005270806.1:p.Asn382=
XM_011541245.1:c.1145A=	XP_011539547.1:p.Asn382=
XM_011541246.1:c.1145A=	XP_011539548.1:p.Asn382=
NM_001127215.2:c.1145A=	NP_001120687.1:p.Asn382=
NM_001127216.2:c.1145A=	NP_001120688.1:p.Asn382=
NM_005263.4:c.1145A=	NP_005254.2:p.Asn382=
XM_011541245.2:c.1145A=	XP_011539547.1:p.Asn382=
XM_011541246.2:c.1145A=	XP_011539548.1:p.Asn382=
NM_005263.5:c.1145A= MANE Select	NP_005254.2:p.Asn382=
NM_001127215.3:c.1145A=	NP_001120687.1:p.Asn382=
NM_001127216.3:c.1145A=	NP_001120688.1:p.Asn382=