Canonical Allele Identifier: CA508272214

Gene: FUT2

Linked Data

• gnomAD v4: 19-48703597-AG-A
• COSMIC: COSM1564331
• MyVariant Identifiers: chr19:g.49206855del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48703602del , CM000681.2:g.48703602del	GRCh38
NC_000019.9:g.49206859del , CM000681.1:g.49206859del	GRCh37
NC_000019.8:g.53898671del	NCBI36
NG_007511.1:g.12632del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425340.3:c.646del MANE Select	ENSP00000387498.2:p.Val216TrpfsTer?
ENST00000522966.2:c.646del	ENSP00000430227.2:p.Val216TrpfsTer?
ENST00000391876.5:c.646del	ENSP00000375748.4:p.Val216TrpfsTer?
ENST00000425340.2:c.646del	ENSP00000387498.2:p.Val216TrpfsTer?
ENST00000522966.1:c.646del	ENSP00000430227.1:p.Val216TrpfsTer?
NM_000511.5:c.646del	NP_000502.4:p.Val216TrpfsTer?
NM_001097638.2:c.646del	NP_001091107.1:p.Val216TrpfsTer?
NR_131188.1:n.251del
NM_000511.6:c.646del MANE Select	NP_000502.4:p.Val216TrpfsTer?
NM_001097638.3:c.646del	NP_001091107.1:p.Val216TrpfsTer?