Canonical Allele Identifier: CA1087498243

Gene: NEU1

Linked Data

• dbSNP Id: rs1762491682
• gnomAD v3: 6-31861173-T-A
• gnomAD v4: 6-31861173-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861173T>A , CM000668.2:g.31861173T>A	GRCh38
NC_000006.11:g.31828950T>A , CM000668.1:g.31828950T>A	GRCh37
NC_000006.10:g.31936929T>A	NCBI36
NG_008201.1:g.6760A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000375631.5:c.615+15A>T MANE Select	ENSP00000364782.4:n.615+15A>T
ENST00000677054.1:n.1307A>T
ENST00000677512.1:n.723+15A>T
ENST00000678869.1:n.738A>T
ENST00000375631.4:c.615+15A>T	ENSP00000364782.4:n.615+15A>T
ENST00000480384.1:n.644+15A>T
ENST00000491768.5:c.615+15A>T	ENSP00000433127.1:n.615+15A>T
ENST00000495807.1:n.1198A>T
NM_000434.3:c.615+15A>T	NP_000425.1:n.615+15A>T
NM_000434.4:c.615+15A>T MANE Select	NP_000425.1:n.615+15A>T