Canonical Allele Identifier: CA363494969

Gene: NEU1

Linked Data

• dbSNP Id: rs1762505257
• gnomAD v4: 6-31861403-G-A
• MyVariant Identifiers: chr6:g.31829180G>A (hg19) ; chr6:g.31861403G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861403G>A , CM000668.2:g.31861403G>A	GRCh38
NC_000006.11:g.31829180G>A , CM000668.1:g.31829180G>A	GRCh37
NC_000006.10:g.31937159G>A	NCBI36
NG_008201.1:g.6530C>T
NG_023058.1:g.22644C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.400C>T MANE Select	ENSP00000364782.4:p.Pro134Ser
ENST00000677054.1:n.1077C>T
ENST00000677512.1:n.508C>T
ENST00000678869.1:n.508C>T
ENST00000375631.4:c.400C>T	ENSP00000364782.4:p.Pro134Ser
ENST00000480384.1:n.429C>T
ENST00000491768.5:c.400C>T	ENSP00000433127.1:p.Pro134Ser
ENST00000495807.1:n.968C>T
NM_000434.3:c.400C>T	NP_000425.1:p.Pro134Ser
NM_000434.4:c.400C>T MANE Select	NP_000425.1:p.Pro134Ser