Canonical Allele Identifier: CA039930

Gene: FUT3

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5844781A>C , CM000681.2:g.5844781A>C	GRCh38
NC_000019.9:g.5844792A>C , CM000681.1:g.5844792A>C	GRCh37
NC_000019.8:g.5795792A>C	NCBI36
NG_007482.1:g.11694T>G
NG_007482.2:g.17342T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303225.12:c.59T>G	ENSP00000305603.5:p.Leu20Arg
ENST00000589620.6:c.59T>G	ENSP00000465804.1:p.Leu20Arg
ENST00000303225.11:c.59T>G	ENSP00000305603.5:p.Leu20Arg
ENST00000458379.7:c.59T>G	ENSP00000416443.1:p.Leu20Arg
ENST00000303225.10:c.59T>G	ENSP00000305603.5:p.Leu20Arg
ENST00000458379.6:c.59T>G	ENSP00000416443.1:p.Leu20Arg
ENST00000585715.1:c.59T>G	ENSP00000467633.1:p.Leu20Arg
ENST00000587048.1:c.59T>G	ENSP00000468515.1:p.Leu20Arg
ENST00000589620.5:c.59T>G	ENSP00000465804.1:p.Leu20Arg
ENST00000589714.1:c.59T>G	ENSP00000467081.1:p.Leu20Arg
ENST00000589918.5:c.59T>G	ENSP00000468123.1:p.Leu20Arg
NM_000149.3:c.59T>G	NP_000140.1:p.Leu20Arg
NM_001097639.1:c.59T>G	NP_001091108.1:p.Leu20Arg
NM_001097640.1:c.59T>G	NP_001091109.1:p.Leu20Arg
NM_001097641.1:c.59T>G	NP_001091110.1:p.Leu20Arg
XM_011527865.1:c.59T>G	XP_011526167.1:p.Leu20Arg
XM_011527866.1:c.59T>G	XP_011526168.1:p.Leu20Arg
XM_011527867.1:c.59T>G	XP_011526169.1:p.Leu20Arg
NM_000149.4:c.59T>G	NP_000140.1:p.Leu20Arg
NM_001097639.3:c.59T>G MANE Select	NP_001091108.3:p.Leu20Arg
NM_001097640.3:c.59T>G	NP_001091109.3:p.Leu20Arg
NM_001097641.3:c.59T>G	NP_001091110.3:p.Leu20Arg
NM_001374740.1:c.59T>G	NP_001361669.1:p.Leu20Arg
NM_001382744.1:c.59T>G	NP_001369673.1:p.Leu20Arg
NM_001382745.1:c.59T>G	NP_001369674.1:p.Leu20Arg
NM_001382746.1:c.59T>G	NP_001369675.1:p.Leu20Arg
NM_001382747.1:c.59T>G	NP_001369676.1:p.Leu20Arg
NM_001382748.1:c.59T>G	NP_001369677.1:p.Leu20Arg
NM_001382749.1:c.59T>G	NP_001369678.1:p.Leu20Arg
NM_001382750.1:c.59T>G	NP_001369679.1:p.Leu20Arg