Canonical Allele Identifier: CA2678053925
Gene: NEU1 HGNC NCBI

Linked Data

gnomAD v4: 6-31861520-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31861520A>C , CM000668.2:g.31861520A>C GRCh38
NC_000006.11:g.31829297A>C , CM000668.1:g.31829297A>C GRCh37
NC_000006.10:g.31937276A>C NCBI36
NG_008201.1:g.6413T>G
NG_023058.1:g.22527T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.353-70T>G MANE Select ENSP00000364782.4:n.353-70T>G
ENST00000677054.1:n.960T>G
ENST00000677512.1:n.461-70T>G
ENST00000678869.1:n.461-70T>G
ENST00000375631.4:c.353-70T>G ENSP00000364782.4:n.353-70T>G
ENST00000480384.1:n.382-70T>G
ENST00000491768.5:c.353-70T>G ENSP00000433127.1:n.353-70T>G
ENST00000495807.1:n.851T>G
NM_000434.3:c.353-70T>G NP_000425.1:n.353-70T>G
NM_000434.4:c.353-70T>G MANE Select NP_000425.1:n.353-70T>G
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