Canonical Allele Identifier: CA2678053923
Gene: NEU1 HGNC NCBI

Linked Data

gnomAD v4: 6-31861496-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31861496T>G , CM000668.2:g.31861496T>G GRCh38
NC_000006.11:g.31829273T>G , CM000668.1:g.31829273T>G GRCh37
NC_000006.10:g.31937252T>G NCBI36
NG_008201.1:g.6437A>C
NG_023058.1:g.22551A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000375631.5:c.353-46A>C MANE Select ENSP00000364782.4:n.353-46A>C
ENST00000677054.1:n.984A>C
ENST00000677512.1:n.461-46A>C
ENST00000678869.1:n.461-46A>C
ENST00000375631.4:c.353-46A>C ENSP00000364782.4:n.353-46A>C
ENST00000480384.1:n.382-46A>C
ENST00000491768.5:c.353-46A>C ENSP00000433127.1:n.353-46A>C
ENST00000495807.1:n.875A>C
NM_000434.3:c.353-46A>C NP_000425.1:n.353-46A>C
NM_000434.4:c.353-46A>C MANE Select NP_000425.1:n.353-46A>C
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