Canonical Allele Identifier: CA449808520

Gene: NEU1

Linked Data

• MyVariant Identifiers: chr6:g.31829046A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861269A>T , CM000668.2:g.31861269A>T	GRCh38
NC_000006.11:g.31829046A>T , CM000668.1:g.31829046A>T	GRCh37
NC_000006.10:g.31937025A>T	NCBI36
NG_008201.1:g.6664T>A
NG_023058.1:g.22778T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.534T>A MANE Select	ENSP00000364782.4:p.Gly178=
ENST00000677054.1:n.1211T>A
ENST00000677512.1:n.642T>A
ENST00000678869.1:n.642T>A
ENST00000375631.4:c.534T>A	ENSP00000364782.4:p.Gly178=
ENST00000480384.1:n.563T>A
ENST00000491768.5:c.534T>A	ENSP00000433127.1:p.Gly178=
ENST00000495807.1:n.1102T>A
NM_000434.3:c.534T>A	NP_000425.1:p.Gly178=
NM_000434.4:c.534T>A MANE Select	NP_000425.1:p.Gly178=