Canonical Allele Identifier: CA2320141868

Gene: FUT3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5844332C= , CM000681.2:g.5844332C=	GRCh38
NC_000019.9:g.5844343C= , CM000681.1:g.5844343C=	GRCh37
NC_000019.8:g.5795343C=	NCBI36
NG_007482.1:g.12143G=
NG_007505.1:g.400G=
NG_007482.2:g.17791G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001097639.3:c.508G= MANE Select	NP_001091108.3:p.Gly170=
NM_000149.3:c.508G=	NP_000140.1:p.Gly170=
NM_000149.4:c.508G=	NP_000140.1:p.Gly170=
NM_001097639.1:c.508G=	NP_001091108.1:p.Gly170=
NM_001097640.1:c.508G=	NP_001091109.1:p.Gly170=
NM_001097640.3:c.508G=	NP_001091109.3:p.Gly170=
NM_001097641.1:c.508G=	NP_001091110.1:p.Gly170=
NM_001097641.3:c.508G=	NP_001091110.3:p.Gly170=
NM_001374740.1:c.508G=	NP_001361669.1:p.Gly170=
NM_001382744.1:c.508G=	NP_001369673.1:p.Gly170=
NM_001382745.1:c.508G=	NP_001369674.1:p.Gly170=
NM_001382746.1:c.508G=	NP_001369675.1:p.Gly170=
NM_001382747.1:c.508G=	NP_001369676.1:p.Gly170=
NM_001382748.1:c.508G=	NP_001369677.1:p.Gly170=
NM_001382749.1:c.508G=	NP_001369678.1:p.Gly170=
NM_001382750.1:c.508G=	NP_001369679.1:p.Gly170=
ENST00000303225.10:c.508G=	ENSP00000305603.5:p.Gly170=
ENST00000303225.11:c.508G=	ENSP00000305603.5:p.Gly170=
ENST00000303225.12:c.508G=	ENSP00000305603.5:p.Gly170=
ENST00000458379.6:c.508G=	ENSP00000416443.1:p.Gly170=
ENST00000458379.7:c.508G=	ENSP00000416443.1:p.Gly170=
ENST00000589620.5:c.508G=	ENSP00000465804.1:p.Gly170=
ENST00000589620.6:c.508G=	ENSP00000465804.1:p.Gly170=
ENST00000589918.5:c.508G=	ENSP00000468123.1:p.Gly170=
XM_011527865.1:c.508G=	XP_011526167.1:p.Gly170=
XM_011527866.1:c.508G=	XP_011526168.1:p.Gly170=
XM_011527867.1:c.508G=	XP_011526169.1:p.Gly170=