Canonical Allele Identifier: CA2143138404

Gene: FUT8

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65471221_65471222delinsCT , CM000676.2:g.65471221_65471222delinsCT	GRCh38
NC_000014.8:g.65937939_65937940delinsCT , CM000676.1:g.65937939_65937940delinsCT	GRCh37
NC_000014.7:g.65007692_65007693delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673929.1:c.-228+15503_-228+15504delinsCT MANE Select	ENSP00000501213.1:n.-228+15503_-228+15504delinsCT
ENST00000674118.1:c.-228+15503_-228+15504delinsCT	ENSP00000501008.1:n.-228+15503_-228+15504delinsCT
ENST00000342677.10:c.-228+15503_-228+15504delinsCT	ENSP00000345865.6:n.-228+15503_-228+15504delinsCT
ENST00000358307.6:c.-287+15503_-287+15504delinsCT	ENSP00000351057.2:n.-287+15503_-287+15504delinsCT
ENST00000360689.9:c.-228+15503_-228+15504delinsCT	ENSP00000353910.5:n.-228+15503_-228+15504delinsCT
ENST00000394586.6:c.-228+59228_-228+59229delinsCT	ENSP00000378087.2:n.-228+59228_-228+59229delinsCT
ENST00000553924.5:c.-374+15503_-374+15504delinsCT	ENSP00000451577.1:n.-374+15503_-374+15504delinsCT
ENST00000554610.1:c.-228+58007_-228+58008delinsCT	ENSP00000452309.1:n.-228+58007_-228+58008delinsCT
ENST00000555559.5:c.-305-8486_-305-8485delinsCT	ENSP00000451689.1:n.-305-8486_-305-8485delinsCT
ENST00000556518.5:c.-228+15503_-228+15504delinsCT	ENSP00000452597.1:n.-228+15503_-228+15504delinsCT
ENST00000557164.5:c.-287+15503_-287+15504delinsCT	ENSP00000452433.1:n.-287+15503_-287+15504delinsCT
ENST00000557338.5:c.-305-8486_-305-8485delinsCT	ENSP00000452105.1:n.-305-8486_-305-8485delinsCT
NM_004480.4:c.-287+15503_-287+15504delinsCT	NP_004471.4:n.-287+15503_-287+15504delinsCT
NM_178155.2:c.-228+15503_-228+15504delinsCT	NP_835368.1:n.-228+15503_-228+15504delinsCT
NM_178156.2:c.-228+59228_-228+59229delinsCT	NP_835369.1:n.-228+59228_-228+59229delinsCT
NR_038167.1:n.1500+15503_1500+15504delinsCT
NR_038170.1:n.583+15503_583+15504delinsCT
XM_011536613.1:c.-228+58007_-228+58008delinsCT	XP_011534915.1:n.-228+58007_-228+58008delinsCT
XM_017021136.1:c.-228+15503_-228+15504delinsCT	XP_016876625.1:n.-228+15503_-228+15504delinsCT
XM_017021137.1:c.-228+15503_-228+15504delinsCT	XP_016876626.1:n.-228+15503_-228+15504delinsCT
XM_017021138.1:c.-228+59228_-228+59229delinsCT	XP_016876627.1:n.-228+59228_-228+59229delinsCT
XM_017021139.1:c.-228+58007_-228+58008delinsCT	XP_016876628.1:n.-228+58007_-228+58008delinsCT
NM_001371533.1:c.-228+15503_-228+15504delinsCT MANE Select	NP_001358462.1:n.-228+15503_-228+15504delinsCT
NM_001371534.1:c.-228+15503_-228+15504delinsCT	NP_001358463.1:n.-228+15503_-228+15504delinsCT
NM_001371536.1:c.-228+15503_-228+15504delinsCT	NP_001358465.1:n.-228+15503_-228+15504delinsCT
NM_178155.3:c.-228+15503_-228+15504delinsCT	NP_835368.1:n.-228+15503_-228+15504delinsCT