Canonical Allele Identifier: CA7233088

Gene: FUT8

Linked Data

• dbSNP Id: rs771905337
• ExAC: 14:65937790 TTGTACAAGAGC / T
• gnomAD v2: 14-65937790-TTGTACAAGAGC-T
• MyVariant Identifiers: chr14:g.65937791_65937801del (hg19) ; chr14:g.65471073_65471083del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65471078_65471088del , CM000676.2:g.65471078_65471088del	GRCh38
NC_000014.8:g.65937796_65937806del , CM000676.1:g.65937796_65937806del	GRCh37
NC_000014.7:g.65007549_65007559del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673929.1:c.-228+15360_-228+15370del MANE Select	ENSP00000501213.1:n.-228+15360_-228+15370del
ENST00000674118.1:c.-228+15360_-228+15370del	ENSP00000501008.1:n.-228+15360_-228+15370del
ENST00000342677.10:c.-228+15360_-228+15370del	ENSP00000345865.6:n.-228+15360_-228+15370del
ENST00000358307.6:c.-287+15360_-287+15370del	ENSP00000351057.2:n.-287+15360_-287+15370del
ENST00000360689.9:c.-228+15360_-228+15370del	ENSP00000353910.5:n.-228+15360_-228+15370del
ENST00000394586.6:c.-228+59085_-228+59095del	ENSP00000378087.2:n.-228+59085_-228+59095del
ENST00000553924.5:c.-374+15360_-374+15370del	ENSP00000451577.1:n.-374+15360_-374+15370del
ENST00000554610.1:c.-228+57864_-228+57874del	ENSP00000452309.1:n.-228+57864_-228+57874del
ENST00000555559.5:c.-305-8629_-305-8619del	ENSP00000451689.1:n.-305-8629_-305-8619del
ENST00000556518.5:c.-228+15360_-228+15370del	ENSP00000452597.1:n.-228+15360_-228+15370del
ENST00000557164.5:c.-287+15360_-287+15370del	ENSP00000452433.1:n.-287+15360_-287+15370del
ENST00000557338.5:c.-305-8629_-305-8619del	ENSP00000452105.1:n.-305-8629_-305-8619del
NM_004480.4:c.-287+15360_-287+15370del	NP_004471.4:n.-287+15360_-287+15370del
NM_178155.2:c.-228+15360_-228+15370del	NP_835368.1:n.-228+15360_-228+15370del
NM_178156.2:c.-228+59085_-228+59095del	NP_835369.1:n.-228+59085_-228+59095del
NR_038167.1:n.1500+15360_1500+15370del
NR_038170.1:n.583+15360_583+15370del
XM_011536613.1:c.-228+57864_-228+57874del	XP_011534915.1:n.-228+57864_-228+57874del
XM_017021136.1:c.-228+15360_-228+15370del	XP_016876625.1:n.-228+15360_-228+15370del
XM_017021137.1:c.-228+15360_-228+15370del	XP_016876626.1:n.-228+15360_-228+15370del
XM_017021138.1:c.-228+59085_-228+59095del	XP_016876627.1:n.-228+59085_-228+59095del
XM_017021139.1:c.-228+57864_-228+57874del	XP_016876628.1:n.-228+57864_-228+57874del
NM_001371533.1:c.-228+15360_-228+15370del MANE Select	NP_001358462.1:n.-228+15360_-228+15370del
NM_001371534.1:c.-228+15360_-228+15370del	NP_001358463.1:n.-228+15360_-228+15370del
NM_001371536.1:c.-228+15360_-228+15370del	NP_001358465.1:n.-228+15360_-228+15370del
NM_178155.3:c.-228+15360_-228+15370del	NP_835368.1:n.-228+15360_-228+15370del