Canonical Allele Identifier: CA2741636653
Gene: FUT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703420_48703421insTCT , CM000681.2:g.48703420_48703421insTCT GRCh38
NC_000019.9:g.49206677_49206678insTCT , CM000681.1:g.49206677_49206678insTCT GRCh37
NC_000019.8:g.53898489_53898490insTCT NCBI36
NG_007511.1:g.12450_12451insTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.464_465insTCT MANE Select ENSP00000387498.2:p.Thr155_Phe156insLeu
ENST00000522966.2:c.464_465insTCT ENSP00000430227.2:p.Thr155_Phe156insLeu
ENST00000391876.5:c.464_465insTCT ENSP00000375748.4:p.Thr155_Phe156insLeu
ENST00000425340.2:c.464_465insTCT ENSP00000387498.2:p.Thr155_Phe156insLeu
ENST00000522966.1:c.464_465insTCT ENSP00000430227.1:p.Thr155_Phe156insLeu
NM_000511.5:c.464_465insTCT NP_000502.4:p.Thr155_Phe156insLeu
NM_001097638.2:c.464_465insTCT NP_001091107.1:p.Thr155_Phe156insLeu
NR_131188.1:n.428_429insAGA
NM_000511.6:c.464_465insTCT MANE Select NP_000502.4:p.Thr155_Phe156insLeu
NM_001097638.3:c.464_465insTCT NP_001091107.1:p.Thr155_Phe156insLeu