Canonical Allele Identifier: CA5559253

Gene: FUT11

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.73773452T>C , CM000672.2:g.73773452T>C	GRCh38
NC_000010.10:g.75533210T>C , CM000672.1:g.75533210T>C	GRCh37
NC_000010.9:g.75203216T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372841.8:c.971T>C MANE Select	ENSP00000361932.3:p.Ile324Thr
ENST00000372841.7:c.971T>C	ENSP00000361932.3:p.Ile324Thr
ENST00000394790.2:c.971T>C	ENSP00000378270.1:p.Ile324Thr
ENST00000465695.1:n.737T>C
NM_001284194.1:c.971T>C	NP_001271123.1:p.Ile324Thr
NM_173540.2:c.971T>C	NP_775811.2:p.Ile324Thr
XM_005269588.2:c.*103T>C	XP_005269645.1:n.*103T>C
XM_006717656.2:c.971T>C	XP_006717719.1:p.Ile324Thr
XM_006717656.4:c.971T>C	XP_006717719.1:p.Ile324Thr
XR_001747049.2:n.1127T>C
XR_001747050.2:n.1127T>C
XR_002956964.1:n.1007T>C
NM_173540.3:c.971T>C MANE Select	NP_775811.2:p.Ile324Thr
NM_001284194.2:c.971T>C	NP_001271123.1:p.Ile324Thr