Canonical Allele Identifier: CA2625298079

Gene: FUT8

Linked Data

• gnomAD v4: 14-65471190-CCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65471191_65471192del , CM000676.2:g.65471191_65471192del	GRCh38
NC_000014.8:g.65937909_65937910del , CM000676.1:g.65937909_65937910del	GRCh37
NC_000014.7:g.65007662_65007663del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673929.1:c.-228+15473_-228+15474del MANE Select	ENSP00000501213.1:n.-228+15473_-228+15474del
ENST00000674118.1:c.-228+15473_-228+15474del	ENSP00000501008.1:n.-228+15473_-228+15474del
ENST00000342677.10:c.-228+15473_-228+15474del	ENSP00000345865.6:n.-228+15473_-228+15474del
ENST00000358307.6:c.-287+15473_-287+15474del	ENSP00000351057.2:n.-287+15473_-287+15474del
ENST00000360689.9:c.-228+15473_-228+15474del	ENSP00000353910.5:n.-228+15473_-228+15474del
ENST00000394586.6:c.-228+59198_-228+59199del	ENSP00000378087.2:n.-228+59198_-228+59199del
ENST00000553924.5:c.-374+15473_-374+15474del	ENSP00000451577.1:n.-374+15473_-374+15474del
ENST00000554610.1:c.-228+57977_-228+57978del	ENSP00000452309.1:n.-228+57977_-228+57978del
ENST00000555559.5:c.-305-8516_-305-8515del	ENSP00000451689.1:n.-305-8516_-305-8515del
ENST00000556518.5:c.-228+15473_-228+15474del	ENSP00000452597.1:n.-228+15473_-228+15474del
ENST00000557164.5:c.-287+15473_-287+15474del	ENSP00000452433.1:n.-287+15473_-287+15474del
ENST00000557338.5:c.-305-8516_-305-8515del	ENSP00000452105.1:n.-305-8516_-305-8515del
NM_004480.4:c.-287+15473_-287+15474del	NP_004471.4:n.-287+15473_-287+15474del
NM_178155.2:c.-228+15473_-228+15474del	NP_835368.1:n.-228+15473_-228+15474del
NM_178156.2:c.-228+59198_-228+59199del	NP_835369.1:n.-228+59198_-228+59199del
NR_038167.1:n.1500+15473_1500+15474del
NR_038170.1:n.583+15473_583+15474del
XM_011536613.1:c.-228+57977_-228+57978del	XP_011534915.1:n.-228+57977_-228+57978del
XM_017021136.1:c.-228+15473_-228+15474del	XP_016876625.1:n.-228+15473_-228+15474del
XM_017021137.1:c.-228+15473_-228+15474del	XP_016876626.1:n.-228+15473_-228+15474del
XM_017021138.1:c.-228+59198_-228+59199del	XP_016876627.1:n.-228+59198_-228+59199del
XM_017021139.1:c.-228+57977_-228+57978del	XP_016876628.1:n.-228+57977_-228+57978del
NM_001371533.1:c.-228+15473_-228+15474del MANE Select	NP_001358462.1:n.-228+15473_-228+15474del
NM_001371534.1:c.-228+15473_-228+15474del	NP_001358463.1:n.-228+15473_-228+15474del
NM_001371536.1:c.-228+15473_-228+15474del	NP_001358465.1:n.-228+15473_-228+15474del
NM_178155.3:c.-228+15473_-228+15474del	NP_835368.1:n.-228+15473_-228+15474del