Canonical Allele Identifier: CA363495166

Gene: NEU1

Linked Data

• MyVariant Identifiers: chr6:g.31829213G>T (hg19) ; chr6:g.31861436G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861436G>T , CM000668.2:g.31861436G>T	GRCh38
NC_000006.11:g.31829213G>T , CM000668.1:g.31829213G>T	GRCh37
NC_000006.10:g.31937192G>T	NCBI36
NG_008201.1:g.6497C>A
NG_023058.1:g.22611C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.367C>A MANE Select	ENSP00000364782.4:p.Pro123Thr
ENST00000677054.1:n.1044C>A
ENST00000677512.1:n.475C>A
ENST00000678869.1:n.475C>A
ENST00000375631.4:c.367C>A	ENSP00000364782.4:p.Pro123Thr
ENST00000480384.1:n.396C>A
ENST00000491768.5:c.367C>A	ENSP00000433127.1:p.Pro123Thr
ENST00000495807.1:n.935C>A
NM_000434.3:c.367C>A	NP_000425.1:p.Pro123Thr
NM_000434.4:c.367C>A MANE Select	NP_000425.1:p.Pro123Thr