Canonical Allele Identifier: CA144124229
Gene: FUT9 HGNC NCBI

Linked Data

dbSNP Id: rs532704041

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96057300_96057303del , CM000668.2:g.96057300_96057303del GRCh38
NC_000006.11:g.96505176_96505179del , CM000668.1:g.96505176_96505179del GRCh37
NC_000006.10:g.96611897_96611900del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000302103.6:c.-98+41088_-98+41091del MANE Select ENSP00000302599.4:n.-98+41088_-98+41091de...
ENST00000302103.5:c.-98+41088_-98+41091del ENSP00000302599.4:n.-98+41088_-98+41091de...
NM_006581.3:c.-98+41088_-98+41091del NP_006572.2:n.-98+41088_-98+41091del
XM_011535384.1:c.-98+36327_-98+36330del XP_011533686.1:n.-98+36327_-98+36330del
XM_017010190.1:c.-215+41088_-215+41091del XP_016865679.1:n.-215+41088_-215+41091del...
XR_001744267.2:n.1955_1958del
NM_006581.4:c.-98+41088_-98+41091del MANE Select NP_006572.2:n.-98+41088_-98+41091del