Canonical Allele Identifier: CA2678053909
Gene: NEU1 HGNC NCBI

Linked Data

gnomAD v4: 6-31861182-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31861182A>C , CM000668.2:g.31861182A>C GRCh38
NC_000006.11:g.31828959A>C , CM000668.1:g.31828959A>C GRCh37
NC_000006.10:g.31936938A>C NCBI36
NG_008201.1:g.6751T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000375631.5:c.615+6T>G MANE Select ENSP00000364782.4:n.615+6T>G
ENST00000677054.1:n.1298T>G
ENST00000677512.1:n.723+6T>G
ENST00000678869.1:n.729T>G
ENST00000375631.4:c.615+6T>G ENSP00000364782.4:n.615+6T>G
ENST00000480384.1:n.644+6T>G
ENST00000491768.5:c.615+6T>G ENSP00000433127.1:n.615+6T>G
ENST00000495807.1:n.1189T>G
NM_000434.3:c.615+6T>G NP_000425.1:n.615+6T>G
NM_000434.4:c.615+6T>G MANE Select NP_000425.1:n.615+6T>G
Search 100 bp 5'
Search 100 bp 3'