Canonical Allele Identifier: CA14741614

Gene: FUT6

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5834201C>T , CM000681.2:g.5834201C>T	GRCh38
NC_000019.9:g.5834212C>T , CM000681.1:g.5834212C>T	GRCh37
NC_000019.8:g.5785212C>T	NCBI36
NG_007505.1:g.10531G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318336.10:c.-13+749G>A MANE Select	ENSP00000313398.4:n.-13+749G>A
ENST00000286955.5:c.-12-1622G>A	ENSP00000286955.5:n.-12-1622G>A
ENST00000318336.8:c.-13+749G>A	ENSP00000313398.4:n.-13+749G>A
ENST00000524754.1:c.-12-1622G>A	ENSP00000431708.1:n.-12-1622G>A
ENST00000527106.5:c.-58+749G>A	ENSP00000432954.1:n.-58+749G>A
ENST00000528505.1:c.-13+749G>A	ENSP00000433811.1:n.-13+749G>A
ENST00000529165.5:c.-13+749G>A	ENSP00000436547.1:n.-13+749G>A
ENST00000531085.5:c.-58+106G>A	ENSP00000432161.1:n.-58+106G>A
ENST00000531199.1:c.-13+639G>A	ENSP00000436413.1:n.-13+639G>A
ENST00000532464.5:c.-13+749G>A	ENSP00000431880.1:n.-13+749G>A
NM_000150.2:c.-13+749G>A	NP_000141.1:n.-13+749G>A
NM_001040701.1:c.-12-1622G>A	NP_001035791.1:n.-12-1622G>A
XM_005259526.3:c.-58+749G>A	XP_005259583.1:n.-58+749G>A
XM_005259527.3:c.-12-1622G>A	XP_005259584.1:n.-12-1622G>A
XM_011527868.1:c.-130+749G>A	XP_011526170.1:n.-130+749G>A
XM_011527869.1:c.-127+749G>A	XP_011526171.1:n.-127+749G>A
XM_011527870.1:c.-58+106G>A	XP_011526172.1:n.-58+106G>A
XM_011527871.1:c.-58+106G>A	XP_011526173.1:n.-58+106G>A
XM_011527872.1:c.-58+749G>A	XP_011526174.1:n.-58+749G>A
XM_011527873.1:c.-13+106G>A	XP_011526175.1:n.-13+106G>A
XM_011527874.1:c.-13+749G>A	XP_011526176.1:n.-13+749G>A
XM_011527875.1:c.-58+749G>A	XP_011526177.1:n.-58+749G>A
XM_011527876.1:c.-13+749G>A	XP_011526178.1:n.-13+749G>A
XM_011527877.1:c.-58+749G>A	XP_011526179.1:n.-58+749G>A
XM_011527878.1:c.-57-1296G>A	XP_011526180.1:n.-57-1296G>A
XM_011527879.1:c.-12-1622G>A	XP_011526181.1:n.-12-1622G>A
XM_005259526.5:c.-58+749G>A	XP_005259583.1:n.-58+749G>A
XM_005259527.4:c.-12-1622G>A	XP_005259584.1:n.-12-1622G>A
XM_011527872.3:c.-58+749G>A	XP_011526174.1:n.-58+749G>A
XM_011527874.3:c.-13+749G>A	XP_011526176.1:n.-13+749G>A
XM_011527875.3:c.-58+749G>A	XP_011526177.1:n.-58+749G>A
XM_011527876.3:c.-13+749G>A	XP_011526178.1:n.-13+749G>A
XM_011527879.3:c.-12-1622G>A	XP_011526181.1:n.-12-1622G>A
NM_001369502.1:c.-58+749G>A	NP_001356431.1:n.-58+749G>A
NM_001369504.1:c.-13+749G>A	NP_001356433.1:n.-13+749G>A
NM_001369505.1:c.-13+749G>A	NP_001356434.1:n.-13+749G>A
NM_000150.4:c.-13+749G>A MANE Select	NP_000141.1:n.-13+749G>A
NM_001040701.2:c.-12-1622G>A	NP_001035791.1:n.-12-1622G>A
NM_001381955.1:c.-12-1622G>A	NP_001368884.1:n.-12-1622G>A
NM_001381956.1:c.-13+749G>A	NP_001368885.1:n.-13+749G>A
NM_001381957.1:c.-12-1622G>A	NP_001368886.1:n.-12-1622G>A
NM_001381958.1:c.-130-77G>A	NP_001368887.1:n.-130-77G>A
NM_001381959.1:c.-13+749G>A	NP_001368888.1:n.-13+749G>A