Canonical Allele Identifier: CA1619342182
Gene: NEU1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31861071A= , CM000668.2:g.31861071A= GRCh38
NC_000006.11:g.31828848A= , CM000668.1:g.31828848A= GRCh37
NC_000006.10:g.31936827A= NCBI36
NG_008201.1:g.6862T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.615+117T= MANE Select ENSP00000364782.4:n.615+117T=
ENST00000677054.1:n.1409T=
ENST00000677512.1:n.723+117T=
ENST00000678869.1:n.840T=
ENST00000375631.4:c.615+117T= ENSP00000364782.4:n.615+117T=
ENST00000480384.1:n.644+117T=
ENST00000491768.5:c.615+117T= ENSP00000433127.1:n.615+117T=
ENST00000495807.1:n.1300T=
NM_000434.3:c.615+117T= NP_000425.1:n.615+117T=
NM_000434.4:c.615+117T= MANE Select NP_000425.1:n.615+117T=
Search 100 bp 5'
Search 100 bp 3'