Canonical Allele Identifier: CA614716319

Gene: FUT8 MIR625

Linked Data

• dbSNP Id: rs1458767783
• gnomAD v2: 14-65937819-A-AG
• gnomAD v4: 14-65471101-A-AG
• MyVariant Identifiers: chr14:g.65937819_65937820insG (hg19) ; chr14:g.65471101_65471102insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65471101_65471102insG , CM000676.2:g.65471101_65471102insG	GRCh38
NC_000014.8:g.65937819_65937820insG , CM000676.1:g.65937819_65937820insG	GRCh37
NC_000014.7:g.65007572_65007573insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673929.1:c.-228+15383_-228+15384insG (FUT8) MANE Select	ENSP00000501213.1:n.-228+15383_-228+15384insG
ENST00000674118.1:c.-228+15383_-228+15384insG (FUT8)	ENSP00000501008.1:n.-228+15383_-228+15384insG
ENST00000342677.10:c.-228+15383_-228+15384insG (FUT8)	ENSP00000345865.6:n.-228+15383_-228+15384insG
ENST00000358307.6:c.-287+15383_-287+15384insG (FUT8)	ENSP00000351057.2:n.-287+15383_-287+15384insG
ENST00000360689.9:c.-228+15383_-228+15384insG (FUT8)	ENSP00000353910.5:n.-228+15383_-228+15384insG
ENST00000394586.6:c.-228+59108_-228+59109insG (FUT8)	ENSP00000378087.2:n.-228+59108_-228+59109insG
ENST00000553924.5:c.-374+15383_-374+15384insG (FUT8)	ENSP00000451577.1:n.-374+15383_-374+15384insG
ENST00000554610.1:c.-228+57887_-228+57888insG (FUT8)	ENSP00000452309.1:n.-228+57887_-228+57888insG
ENST00000555559.5:c.-305-8606_-305-8605insG (FUT8)	ENSP00000451689.1:n.-305-8606_-305-8605insG
ENST00000556518.5:c.-228+15383_-228+15384insG (FUT8)	ENSP00000452597.1:n.-228+15383_-228+15384insG
ENST00000557164.5:c.-287+15383_-287+15384insG (FUT8)	ENSP00000452433.1:n.-287+15383_-287+15384insG
ENST00000557338.5:c.-305-8606_-305-8605insG (FUT8)	ENSP00000452105.1:n.-305-8606_-305-8605insG
NM_004480.4:c.-287+15383_-287+15384insG (FUT8)	NP_004471.4:n.-287+15383_-287+15384insG
NM_178155.2:c.-228+15383_-228+15384insG (FUT8)	NP_835368.1:n.-228+15383_-228+15384insG
NM_178156.2:c.-228+59108_-228+59109insG (FUT8)	NP_835369.1:n.-228+59108_-228+59109insG
NR_030355.1:n.1-1_1insG (MIR625)
NR_038167.1:n.1500+15383_1500+15384insG (FUT8)
NR_038170.1:n.583+15383_583+15384insG (FUT8)
XM_011536613.1:c.-228+57887_-228+57888insG (FUT8)	XP_011534915.1:n.-228+57887_-228+57888insG
XM_017021136.1:c.-228+15383_-228+15384insG (FUT8)	XP_016876625.1:n.-228+15383_-228+15384insG
XM_017021137.1:c.-228+15383_-228+15384insG (FUT8)	XP_016876626.1:n.-228+15383_-228+15384insG
XM_017021138.1:c.-228+59108_-228+59109insG (FUT8)	XP_016876627.1:n.-228+59108_-228+59109insG
XM_017021139.1:c.-228+57887_-228+57888insG (FUT8)	XP_016876628.1:n.-228+57887_-228+57888insG
NM_001371533.1:c.-228+15383_-228+15384insG (FUT8) MANE Select	NP_001358462.1:n.-228+15383_-228+15384insG
NM_001371534.1:c.-228+15383_-228+15384insG (FUT8)	NP_001358463.1:n.-228+15383_-228+15384insG
NM_001371536.1:c.-228+15383_-228+15384insG (FUT8)	NP_001358465.1:n.-228+15383_-228+15384insG
NM_178155.3:c.-228+15383_-228+15384insG (FUT8)	NP_835368.1:n.-228+15383_-228+15384insG