Canonical Allele Identifier: CA2578570785
Gene: NEU1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31861497A>G , CM000668.2:g.31861497A>G GRCh38
NC_000006.11:g.31829274A>G , CM000668.1:g.31829274A>G GRCh37
NC_000006.10:g.31937253A>G NCBI36
NG_008201.1:g.6436T>C
NG_023058.1:g.22550T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.353-47T>C MANE Select ENSP00000364782.4:n.353-47T>C
ENST00000677054.1:n.983T>C
ENST00000677512.1:n.461-47T>C
ENST00000678869.1:n.461-47T>C
ENST00000375631.4:c.353-47T>C ENSP00000364782.4:n.353-47T>C
ENST00000480384.1:n.382-47T>C
ENST00000491768.5:c.353-47T>C ENSP00000433127.1:n.353-47T>C
ENST00000495807.1:n.874T>C
NM_000434.3:c.353-47T>C NP_000425.1:n.353-47T>C
NM_000434.4:c.353-47T>C MANE Select NP_000425.1:n.353-47T>C
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